esv2678177

Organism: Homo sapiens

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

Variant Calls:34
Validation:Yes
Clinical Assertions: No
Region Size:7,448

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: 344 SVs from 69 studies. See in: genome view

Remapped(Score: Perfect):222,200,603-222,208,050

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
esv2678177	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
esv2678177	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
essv5433275	deletion	SAMN00000484	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	848
essv5440343	deletion	SAMN00001586	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,356
essv5507952	deletion	SAMN00001587	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,494
essv5585252	deletion	SAMN00001584	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,421
essv5591984	deletion	SAMN00001630	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,448
essv5607551	deletion	SAMN00001628	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,528
essv5630037	deletion	SAMN00000573	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,195
essv5668972	deletion	SAMN00001669	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,589
essv5677904	deletion	SAMN00001691	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	803
essv5710611	deletion	SAMN00001578	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,497
essv5734905	deletion	SAMN00001626	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,427
essv5781525	deletion	SAMN00001697	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,511
essv5911509	deletion	SAMN00001686	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	807
essv5954820	deletion	SAMN00001629	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,430
essv5987164	deletion	SAMN00000481	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	950
essv6000733	deletion	SAMN00001624	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,608
essv6003748	deletion	SAMN00001590	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,510
essv6009443	deletion	SAMN00001582	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,248
essv6062070	deletion	SAMN00001632	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,311
essv6077637	deletion	SAMN00001681	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	791
essv6156287	deletion	SAMN00001688	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	843
essv6163082	deletion	SAMN00001581	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,469
essv6172774	deletion	SAMN00000572	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,233
essv6182528	deletion	SAMN00000549	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,136
essv6187743	deletion	SAMN00001576	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,882
essv6204314	deletion	SAMN00001591	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,475
essv6271837	deletion	SAMN00001625	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,265
essv6274635	deletion	SAMN00000480	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	937
essv6403910	deletion	SAMN00001671	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,447
essv6433068	deletion	SAMN00001631	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,164
essv6464846	deletion	SAMN00001685	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,589
essv6492109	deletion	SAMN00001690	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	805
essv6571125	deletion	SAMN00000566	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	947
essv6597048	deletion	SAMN00000475	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	1,658

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
essv5433275	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv5440343	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv5507952	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv5585252	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv5591984	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv5607551	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv5630037	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv5668972	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv5677904	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv5710611	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv5734905	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv5781525	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv5911509	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv5954820	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv5987164	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv6000733	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv6003748	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv6009443	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv6062070	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv6077637	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv6156287	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv6163082	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv6172774	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv6182528	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv6187743	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv6204314	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv6271837	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv6274635	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv6403910	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv6433068	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv6464846	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv6492109	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv6571125	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv6597048	Remapped	Perfect	NC_000001.11:g.(22 2200603_222200974) _(222207680_222208 050)del	GRCh38.p12	First Pass	NC_000001.11	Chr1	222,200,603	222,200,974	222,207,680	222,208,050
essv5433275	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392
essv5440343	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392
essv5507952	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392
essv5585252	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392
essv5591984	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392
essv5607551	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392
essv5630037	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392
essv5668972	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392
essv5677904	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392
essv5710611	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392
essv5734905	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392
essv5781525	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392
essv5911509	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392
essv5954820	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392
essv5987164	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392
essv6000733	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392
essv6003748	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392
essv6009443	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392
essv6062070	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392
essv6077637	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392
essv6156287	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392
essv6163082	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392
essv6172774	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392
essv6182528	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392
essv6187743	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392
essv6204314	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392
essv6271837	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392
essv6274635	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392
essv6403910	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392
essv6433068	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392
essv6464846	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392
essv6492109	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392
essv6571125	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392
essv6597048	Submitted genomic		NC_000001.10:g.(22 2373945_222374316) _(222381022_222381 392)del	GRCh37 (hg19)		NC_000001.10	Chr1	222,373,945	222,374,316	222,381,022	222,381,392

Validation Information

Variant Call ID	Experiment ID	Sample ID	Method	Analysis	Result
essv6597048	7	SAMN00000475	SNP array	Probe signal intensity	Pass
essv6274635	7	SAMN00000480	SNP array	Probe signal intensity	Pass
essv5987164	7	SAMN00000481	SNP array	Probe signal intensity	Pass
essv5433275	7	SAMN00000484	SNP array	Probe signal intensity	Pass
essv6182528	7	SAMN00000549	SNP array	Probe signal intensity	Pass
essv6571125	7	SAMN00000566	SNP array	Probe signal intensity	Pass
essv6172774	7	SAMN00000572	SNP array	Probe signal intensity	Pass
essv5630037	7	SAMN00000573	SNP array	Probe signal intensity	Pass
essv6187743	7	SAMN00001576	SNP array	Probe signal intensity	Pass
essv5710611	7	SAMN00001578	SNP array	Probe signal intensity	Pass
essv6163082	7	SAMN00001581	SNP array	Probe signal intensity	Pass
essv6009443	7	SAMN00001582	SNP array	Probe signal intensity	Pass
essv5585252	7	SAMN00001584	SNP array	Probe signal intensity	Pass
essv5440343	7	SAMN00001586	SNP array	Probe signal intensity	Pass
essv5507952	7	SAMN00001587	SNP array	Probe signal intensity	Pass
essv6003748	7	SAMN00001590	SNP array	Probe signal intensity	Pass
essv6204314	7	SAMN00001591	SNP array	Probe signal intensity	Pass
essv6000733	7	SAMN00001624	SNP array	Probe signal intensity	Pass
essv6271837	7	SAMN00001625	SNP array	Probe signal intensity	Pass
essv5734905	7	SAMN00001626	SNP array	Probe signal intensity	Pass
essv5607551	7	SAMN00001628	SNP array	Probe signal intensity	Pass
essv5954820	7	SAMN00001629	SNP array	Probe signal intensity	Pass
essv5591984	7	SAMN00001630	SNP array	Probe signal intensity	Pass
essv6433068	7	SAMN00001631	SNP array	Probe signal intensity	Pass
essv6062070	7	SAMN00001632	SNP array	Probe signal intensity	Pass
essv5668972	7	SAMN00001669	SNP array	Probe signal intensity	Pass
essv6403910	7	SAMN00001671	SNP array	Probe signal intensity	Pass
essv6077637	7	SAMN00001681	SNP array	Probe signal intensity	Pass
essv6464846	7	SAMN00001685	SNP array	Probe signal intensity	Pass
essv5911509	7	SAMN00001686	SNP array	Probe signal intensity	Pass
essv6156287	7	SAMN00001688	SNP array	Probe signal intensity	Pass
essv6492109	7	SAMN00001690	SNP array	Probe signal intensity	Pass
essv5677904	7	SAMN00001691	SNP array	Probe signal intensity	Pass
essv5781525	7	SAMN00001697	SNP array	Probe signal intensity	Pass

dbVar

Database of genomic structural variation

esv2678177

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