Variant Details

Variant: esv3626921

Internal ID

7013751

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr11:79679407..79684846	hg38	UCSC Ensembl
Inner	chr11:79679510..79684708	hg38	UCSC Ensembl
Outer	chr11:79679153..79685100	hg38	UCSC Ensembl
	chr11:79390451..79395890	hg19	UCSC Ensembl
Inner	chr11:79390554..79395752	hg19	UCSC Ensembl
Outer	chr11:79390197..79396144	hg19	UCSC Ensembl

Cytoband

11q14.1

Allele length

Assembly	Allele length
hg38	5440
hg19	5440

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv14216019, essv14216020, essv14216039, essv14216035, essv14216027, essv14216007, essv14216051, essv14216033, essv14216045, essv14216038, essv14216040, essv14216046, essv14216044, essv14216010, essv14216049, essv14216050, essv14216025, essv14216012, essv14216034, essv14216008, essv14216032, essv14216042, essv14216011, essv14216023, essv14216043, essv14216022, essv14216013, essv14216009, essv14216021, essv14216052, essv14216037, essv14216016, essv14216048, essv14216029, essv14216031, essv14216024, essv14216017, essv14216026, essv14216018, essv14216028, essv14216015, essv14216047, essv14216036, essv14216030, essv14216014, essv14216041

Samples

HG03096, HG02339, HG03121, NA18917, HG03280, NA20294, HG03190, NA18504, HG03139, NA19190, HG03095, HG03572, NA19198, NA19923, HG02642, NA19036, HG03058, NA18908, HG03394, HG03048, HG00739, HG02879, HG02819, HG02479, NA19437, NA19175, HG03291, HG01882, HG02322, HG03457, HG02014, HG03123, NA19114, HG02429, NA18856, NA18853, HG03117, NA19360, NA19472, HG03410, NA19096, HG02851, NA19429, NA19346, HG03166, NA19676

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3626921

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	46
Observed Complex	0
Frequency	n/a