esv2670760

Organism: Homo sapiens

Study:estd199 (1000 Genomes Consortium Phase 1)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37 (hg19)

Variant Calls:36
Validation:Yes
Clinical Assertions: No
Region Size:16,848

Publication(s):1000 Genomes Project Consortium et al. 2012

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 482 SVs from 78 studies. See in: genome view

Remapped(Score: Perfect):100,728,772-100,745,619

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
esv2670760	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
esv2670760	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
essv5444817	deletion	SAMN00006472	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,467
essv5452768	deletion	SAMN00006522	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,660
essv5463992	deletion	SAMN00006448	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,788
essv5503955	deletion	SAMN00006531	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,141
essv5505403	deletion	SAMN00006553	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,677
essv5603270	deletion	SAMN00006526	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,211
essv5618825	deletion	SAMN00006516	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,263
essv5654205	deletion	SAMN00006513	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,611
essv5665772	deletion	SAMN00006492	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,011
essv5702995	deletion	SAMN00006447	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,673
essv5869698	deletion	SAMN00006552	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,667
essv5885358	deletion	SAMN00006439	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,754
essv5904103	deletion	SAMN00006487	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,553
essv5910808	deletion	SAMN00006541	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,690
essv5975205	deletion	SAMN00006547	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,684
essv6035333	deletion	SAMN00006445	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,718
essv6051711	deletion	SAMN00006525	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,128
essv6079892	deletion	SAMN00006508	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,015
essv6086107	deletion	SAMN00006504	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,667
essv6153682	deletion	SAMN00006432	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,127
essv6155820	deletion	SAMN00006456	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,686
essv6158491	deletion	SAMN00006505	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,623
essv6189028	deletion	SAMN00006490	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,074
essv6197821	deletion	SAMN00006471	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,344
essv6265013	deletion	SAMN00006469	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,602
essv6266537	deletion	SAMN00006574	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,770
essv6268480	deletion	SAMN00006514	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,671
essv6280820	deletion	SAMN00004690	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,700
essv6293819	deletion	SAMN00006568	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,726
essv6308598	deletion	SAMN00004696	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,778
essv6392263	deletion	SAMN00006532	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,169
essv6446168	deletion	SAMN00006511	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,159
essv6450670	deletion	SAMN00006529	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,277
essv6537831	deletion	SAMN00006558	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,756
essv6538613	deletion	SAMN00006480	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,600
essv6577876	deletion	SAMN00006433	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,373

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
essv5444817	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv5452768	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv5463992	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv5503955	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv5505403	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv5603270	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv5618825	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv5654205	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv5665772	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv5702995	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv5869698	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv5885358	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv5904103	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv5910808	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv5975205	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv6035333	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv6051711	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv6079892	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv6086107	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv6153682	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv6155820	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv6158491	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv6189028	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv6197821	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv6265013	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv6266537	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv6268480	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv6280820	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv6293819	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv6308598	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv6392263	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv6446168	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv6450670	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv6537831	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv6538613	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv6577876	Remapped	Perfect	NC_000007.14:g.(10 0728772_100729143) _(100745249_100745 619)del	GRCh38.p12	First Pass	NC_000007.14	Chr7	100,728,772	100,729,143	100,745,249	100,745,619
essv5444817	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv5452768	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv5463992	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv5503955	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv5505403	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv5603270	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv5618825	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv5654205	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv5665772	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv5702995	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv5869698	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv5885358	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv5904103	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv5910808	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv5975205	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv6035333	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv6051711	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv6079892	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv6086107	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv6153682	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv6155820	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv6158491	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv6189028	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv6197821	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv6265013	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv6266537	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv6268480	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv6280820	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv6293819	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv6308598	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv6392263	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv6446168	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv6450670	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv6537831	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv6538613	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242
essv6577876	Submitted genomic		NC_000007.13:g.(10 0326395_100326766) _(100342872_100343 242)del	GRCh37 (hg19)		NC_000007.13	Chr7	100,326,395	100,326,766	100,342,872	100,343,242

Validation Information

Variant Call ID	Experiment ID	Sample ID	Method	Analysis	Result
essv6280820	9	SAMN00004690	Oligo aCGH	Probe signal intensity	Pass
essv6308598	9	SAMN00004696	Oligo aCGH	Probe signal intensity	Pass
essv6153682	9	SAMN00006432	Oligo aCGH	Probe signal intensity	Pass
essv6577876	9	SAMN00006433	Oligo aCGH	Probe signal intensity	Pass
essv5885358	9	SAMN00006439	Oligo aCGH	Probe signal intensity	Pass
essv6035333	9	SAMN00006445	Oligo aCGH	Probe signal intensity	Pass
essv5702995	9	SAMN00006447	Oligo aCGH	Probe signal intensity	Pass
essv5463992	9	SAMN00006448	Oligo aCGH	Probe signal intensity	Pass
essv6155820	9	SAMN00006456	Oligo aCGH	Probe signal intensity	Pass
essv6265013	9	SAMN00006469	Oligo aCGH	Probe signal intensity	Pass
essv6197821	9	SAMN00006471	Oligo aCGH	Probe signal intensity	Pass
essv5444817	9	SAMN00006472	Oligo aCGH	Probe signal intensity	Pass
essv6538613	9	SAMN00006480	Oligo aCGH	Probe signal intensity	Pass
essv5904103	9	SAMN00006487	Oligo aCGH	Probe signal intensity	Pass
essv6189028	9	SAMN00006490	Oligo aCGH	Probe signal intensity	Pass
essv5665772	9	SAMN00006492	Oligo aCGH	Probe signal intensity	Pass
essv6086107	9	SAMN00006504	Oligo aCGH	Probe signal intensity	Pass
essv6158491	9	SAMN00006505	Oligo aCGH	Probe signal intensity	Pass
essv6079892	9	SAMN00006508	Oligo aCGH	Probe signal intensity	Pass
essv6446168	9	SAMN00006511	Oligo aCGH	Probe signal intensity	Pass
essv5654205	9	SAMN00006513	Oligo aCGH	Probe signal intensity	Pass
essv6268480	9	SAMN00006514	Oligo aCGH	Probe signal intensity	Pass
essv5618825	9	SAMN00006516	Oligo aCGH	Probe signal intensity	Pass
essv5452768	9	SAMN00006522	Oligo aCGH	Probe signal intensity	Pass
essv6051711	9	SAMN00006525	Oligo aCGH	Probe signal intensity	Pass
essv5603270	9	SAMN00006526	Oligo aCGH	Probe signal intensity	Pass
essv6450670	9	SAMN00006529	Oligo aCGH	Probe signal intensity	Pass
essv5503955	9	SAMN00006531	Oligo aCGH	Probe signal intensity	Pass
essv6392263	9	SAMN00006532	Oligo aCGH	Probe signal intensity	Pass
essv5910808	9	SAMN00006541	Oligo aCGH	Probe signal intensity	Pass
essv5975205	9	SAMN00006547	Oligo aCGH	Probe signal intensity	Pass
essv5869698	9	SAMN00006552	Oligo aCGH	Probe signal intensity	Pass
essv5505403	9	SAMN00006553	Oligo aCGH	Probe signal intensity	Pass
essv6537831	9	SAMN00006558	Oligo aCGH	Probe signal intensity	Pass
essv6293819	9	SAMN00006568	Oligo aCGH	Probe signal intensity	Pass
essv6266537	9	SAMN00006574	Oligo aCGH	Probe signal intensity	Pass
essv6280820	7	SAMN00004690	SNP array	Probe signal intensity	Pass
essv6308598	7	SAMN00004696	SNP array	Probe signal intensity	Pass
essv6153682	7	SAMN00006432	SNP array	Probe signal intensity	Pass
essv6577876	7	SAMN00006433	SNP array	Probe signal intensity	Pass
essv5885358	7	SAMN00006439	SNP array	Probe signal intensity	Pass
essv6035333	7	SAMN00006445	SNP array	Probe signal intensity	Pass
essv5702995	7	SAMN00006447	SNP array	Probe signal intensity	Pass
essv5463992	7	SAMN00006448	SNP array	Probe signal intensity	Pass
essv6155820	7	SAMN00006456	SNP array	Probe signal intensity	Pass
essv6265013	7	SAMN00006469	SNP array	Probe signal intensity	Pass
essv6197821	7	SAMN00006471	SNP array	Probe signal intensity	Pass
essv5444817	7	SAMN00006472	SNP array	Probe signal intensity	Pass
essv6538613	7	SAMN00006480	SNP array	Probe signal intensity	Pass
essv5904103	7	SAMN00006487	SNP array	Probe signal intensity	Pass
essv6189028	7	SAMN00006490	SNP array	Probe signal intensity	Pass
essv5665772	7	SAMN00006492	SNP array	Probe signal intensity	Pass
essv6086107	7	SAMN00006504	SNP array	Probe signal intensity	Pass
essv6158491	7	SAMN00006505	SNP array	Probe signal intensity	Pass
essv6079892	7	SAMN00006508	SNP array	Probe signal intensity	Pass
essv6446168	7	SAMN00006511	SNP array	Probe signal intensity	Pass
essv5654205	7	SAMN00006513	SNP array	Probe signal intensity	Pass
essv6268480	7	SAMN00006514	SNP array	Probe signal intensity	Pass
essv5618825	7	SAMN00006516	SNP array	Probe signal intensity	Pass
essv5452768	7	SAMN00006522	SNP array	Probe signal intensity	Pass
essv6051711	7	SAMN00006525	SNP array	Probe signal intensity	Pass
essv5603270	7	SAMN00006526	SNP array	Probe signal intensity	Pass
essv6450670	7	SAMN00006529	SNP array	Probe signal intensity	Pass
essv5503955	7	SAMN00006531	SNP array	Probe signal intensity	Pass
essv6392263	7	SAMN00006532	SNP array	Probe signal intensity	Pass
essv5910808	7	SAMN00006541	SNP array	Probe signal intensity	Pass
essv5975205	7	SAMN00006547	SNP array	Probe signal intensity	Pass
essv5869698	7	SAMN00006552	SNP array	Probe signal intensity	Pass
essv5505403	7	SAMN00006553	SNP array	Probe signal intensity	Pass
essv6537831	7	SAMN00006558	SNP array	Probe signal intensity	Pass
essv6293819	7	SAMN00006568	SNP array	Probe signal intensity	Pass
essv6266537	7	SAMN00006574	SNP array	Probe signal intensity	Pass

dbVar

Database of genomic structural variation

esv2670760

Links to Other Resources

Genome View

Variant Region Placement Information

Variant Call Information

Variant Call Placement Information

Validation Information

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant