esv2656977

Organism: Homo sapiens

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

Variant Calls:38
Validation:Yes
Clinical Assertions: No
Region Size:10,748

Description:High quality site
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: 375 SVs from 54 studies. See in: genome view

Remapped(Score: Perfect):548,645-559,392

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
esv2656977	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
esv2656977	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000019.9	Chr19	548,645	549,016	559,022	559,392

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
essv5421186	deletion	SAMN00001190	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,291
essv5467748	deletion	SAMN00001180	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,453
essv5514906	deletion	SAMN00001162	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,432
essv5547118	deletion	SAMN00001146	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,412
essv5562669	deletion	SAMN00001165	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,213
essv5587885	deletion	SAMN00001185	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,819
essv5648095	deletion	SAMN00001188	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,129
essv5654563	deletion	SAMN00001187	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,291
essv5671566	deletion	SAMN00001189	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,771
essv5717165	deletion	SAMN00001163	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,404
essv5731064	deletion	SAMN00001181	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,016
essv5783386	deletion	SAMN00001182	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,509
essv5810320	deletion	SAMN00001160	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,151
essv5813933	deletion	SAMN00001193	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,179
essv5979878	deletion	SAMN00001170	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,684
essv5991438	deletion	SAMN00001101	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,545
essv6003671	deletion	SAMN00001159	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,248
essv6078306	deletion	SAMN00001172	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,516
essv6090872	deletion	SAMN00001166	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,284
essv6126392	deletion	SAMN00001191	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,461
essv6170646	deletion	SAMN00001129	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,603
essv6178453	deletion	SAMN00001183	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,354
essv6187210	deletion	SAMN00001168	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,626
essv6209830	deletion	SAMN00001173	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,274
essv6257853	deletion	SAMN00001164	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,515
essv6285020	deletion	SAMN00001126	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,684
essv6317731	deletion	SAMN00001176	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,261
essv6359771	deletion	SAMN00001119	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	912
essv6391672	deletion	SAMN00001174	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,500
essv6402289	deletion	SAMN00001177	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,531
essv6403839	deletion	SAMN00001121	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,383
essv6443654	deletion	SAMN00001102	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,259
essv6449900	deletion	SAMN00001186	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,212
essv6483338	deletion	SAMN00001184	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,618
essv6486905	deletion	SAMN00001178	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,252
essv6490039	deletion	SAMN00001122	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,437
essv6562022	deletion	SAMN00001192	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,334
essv6564981	deletion	SAMN00001158	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,358

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
essv5421186	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv5467748	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv5514906	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv5547118	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv5562669	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv5587885	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv5648095	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv5654563	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv5671566	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv5717165	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv5731064	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv5783386	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv5810320	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv5813933	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv5979878	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv5991438	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv6003671	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv6078306	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv6090872	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv6126392	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv6170646	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv6178453	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv6187210	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv6209830	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv6257853	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv6285020	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv6317731	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv6359771	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv6391672	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv6402289	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv6403839	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv6443654	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv6449900	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv6483338	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv6486905	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv6490039	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv6562022	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv6564981	Remapped	Perfect	NC_000019.10:g.(54 8645_549016)_(5590 22_559392)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	548,645	549,016	559,022	559,392
essv5421186	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv5467748	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv5514906	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv5547118	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv5562669	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv5587885	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv5648095	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv5654563	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv5671566	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv5717165	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv5731064	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv5783386	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv5810320	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv5813933	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv5979878	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv5991438	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv6003671	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv6078306	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv6090872	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv6126392	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv6170646	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv6178453	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv6187210	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv6209830	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv6257853	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv6285020	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv6317731	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv6359771	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv6391672	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv6402289	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv6403839	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv6443654	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv6449900	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv6483338	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv6486905	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv6490039	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv6562022	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392
essv6564981	Submitted genomic		NC_000019.9:g.(548 645_549016)_(55902 2_559392)del	GRCh37 (hg19)		NC_000019.9	Chr19	548,645	549,016	559,022	559,392

Validation Information

Variant Call ID	Experiment ID	Sample ID	Method	Analysis	Result
essv5991438	9	SAMN00001101	Oligo aCGH	Probe signal intensity	Pass
essv6443654	9	SAMN00001102	Oligo aCGH	Probe signal intensity	Pass
essv6359771	9	SAMN00001119	Oligo aCGH	Probe signal intensity	Pass
essv6403839	9	SAMN00001121	Oligo aCGH	Probe signal intensity	Pass
essv6490039	9	SAMN00001122	Oligo aCGH	Probe signal intensity	Pass
essv6285020	9	SAMN00001126	Oligo aCGH	Probe signal intensity	Pass
essv6170646	9	SAMN00001129	Oligo aCGH	Probe signal intensity	Pass
essv5547118	9	SAMN00001146	Oligo aCGH	Probe signal intensity	Pass
essv6564981	9	SAMN00001158	Oligo aCGH	Probe signal intensity	Pass
essv6003671	9	SAMN00001159	Oligo aCGH	Probe signal intensity	Pass
essv5810320	9	SAMN00001160	Oligo aCGH	Probe signal intensity	Pass
essv5514906	9	SAMN00001162	Oligo aCGH	Probe signal intensity	Pass
essv5717165	9	SAMN00001163	Oligo aCGH	Probe signal intensity	Pass
essv6257853	9	SAMN00001164	Oligo aCGH	Probe signal intensity	Pass
essv5562669	9	SAMN00001165	Oligo aCGH	Probe signal intensity	Pass
essv6090872	9	SAMN00001166	Oligo aCGH	Probe signal intensity	Pass
essv6187210	9	SAMN00001168	Oligo aCGH	Probe signal intensity	Pass
essv5979878	9	SAMN00001170	Oligo aCGH	Probe signal intensity	Pass
essv6078306	9	SAMN00001172	Oligo aCGH	Probe signal intensity	Pass
essv6209830	9	SAMN00001173	Oligo aCGH	Probe signal intensity	Pass
essv6391672	9	SAMN00001174	Oligo aCGH	Probe signal intensity	Pass
essv6317731	9	SAMN00001176	Oligo aCGH	Probe signal intensity	Pass
essv6402289	9	SAMN00001177	Oligo aCGH	Probe signal intensity	Pass
essv6486905	9	SAMN00001178	Oligo aCGH	Probe signal intensity	Pass
essv5467748	9	SAMN00001180	Oligo aCGH	Probe signal intensity	Pass
essv5731064	9	SAMN00001181	Oligo aCGH	Probe signal intensity	Pass
essv5783386	9	SAMN00001182	Oligo aCGH	Probe signal intensity	Pass
essv6178453	9	SAMN00001183	Oligo aCGH	Probe signal intensity	Pass
essv6483338	9	SAMN00001184	Oligo aCGH	Probe signal intensity	Pass
essv5587885	9	SAMN00001185	Oligo aCGH	Probe signal intensity	Pass
essv6449900	9	SAMN00001186	Oligo aCGH	Probe signal intensity	Pass
essv5654563	9	SAMN00001187	Oligo aCGH	Probe signal intensity	Pass
essv5648095	9	SAMN00001188	Oligo aCGH	Probe signal intensity	Pass
essv5671566	9	SAMN00001189	Oligo aCGH	Probe signal intensity	Pass
essv5421186	9	SAMN00001190	Oligo aCGH	Probe signal intensity	Pass
essv6126392	9	SAMN00001191	Oligo aCGH	Probe signal intensity	Pass
essv6562022	9	SAMN00001192	Oligo aCGH	Probe signal intensity	Pass
essv5813933	9	SAMN00001193	Oligo aCGH	Probe signal intensity	Pass
essv5991438	7	SAMN00001101	SNP array	Probe signal intensity	Pass
essv6443654	7	SAMN00001102	SNP array	Probe signal intensity	Pass
essv6359771	7	SAMN00001119	SNP array	Probe signal intensity	Pass
essv6403839	7	SAMN00001121	SNP array	Probe signal intensity	Pass
essv6490039	7	SAMN00001122	SNP array	Probe signal intensity	Pass
essv6285020	7	SAMN00001126	SNP array	Probe signal intensity	Pass
essv6170646	7	SAMN00001129	SNP array	Probe signal intensity	Pass
essv5547118	7	SAMN00001146	SNP array	Probe signal intensity	Pass
essv6564981	7	SAMN00001158	SNP array	Probe signal intensity	Pass
essv6003671	7	SAMN00001159	SNP array	Probe signal intensity	Pass
essv5810320	7	SAMN00001160	SNP array	Probe signal intensity	Pass
essv5514906	7	SAMN00001162	SNP array	Probe signal intensity	Pass
essv5717165	7	SAMN00001163	SNP array	Probe signal intensity	Pass
essv6257853	7	SAMN00001164	SNP array	Probe signal intensity	Pass
essv5562669	7	SAMN00001165	SNP array	Probe signal intensity	Pass
essv6090872	7	SAMN00001166	SNP array	Probe signal intensity	Pass
essv6187210	7	SAMN00001168	SNP array	Probe signal intensity	Pass
essv5979878	7	SAMN00001170	SNP array	Probe signal intensity	Pass
essv6078306	7	SAMN00001172	SNP array	Probe signal intensity	Pass
essv6209830	7	SAMN00001173	SNP array	Probe signal intensity	Pass
essv6391672	7	SAMN00001174	SNP array	Probe signal intensity	Pass
essv6317731	7	SAMN00001176	SNP array	Probe signal intensity	Pass
essv6402289	7	SAMN00001177	SNP array	Probe signal intensity	Pass
essv6486905	7	SAMN00001178	SNP array	Probe signal intensity	Pass
essv5467748	7	SAMN00001180	SNP array	Probe signal intensity	Pass
essv5731064	7	SAMN00001181	SNP array	Probe signal intensity	Pass
essv5783386	7	SAMN00001182	SNP array	Probe signal intensity	Pass
essv6178453	7	SAMN00001183	SNP array	Probe signal intensity	Pass
essv6483338	7	SAMN00001184	SNP array	Probe signal intensity	Pass
essv5587885	7	SAMN00001185	SNP array	Probe signal intensity	Pass
essv6449900	7	SAMN00001186	SNP array	Probe signal intensity	Pass
essv5654563	7	SAMN00001187	SNP array	Probe signal intensity	Pass
essv5648095	7	SAMN00001188	SNP array	Probe signal intensity	Pass
essv5671566	7	SAMN00001189	SNP array	Probe signal intensity	Pass
essv5421186	7	SAMN00001190	SNP array	Probe signal intensity	Pass
essv6126392	7	SAMN00001191	SNP array	Probe signal intensity	Pass
essv6562022	7	SAMN00001192	SNP array	Probe signal intensity	Pass
essv5813933	7	SAMN00001193	SNP array	Probe signal intensity	Pass

dbVar

Database of genomic structural variation

esv2656977

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