Variant Details

Variant: esv3613620

Internal ID

6653829

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr7:71154728..71159926	hg38	UCSC Ensembl
Inner	chr7:71154728..71159926	hg38	UCSC Ensembl
Outer	chr7:71154386..71160221	hg38	UCSC Ensembl
	chr7:70619714..70624912	hg19	UCSC Ensembl
Inner	chr7:70619714..70624912	hg19	UCSC Ensembl
Outer	chr7:70619372..70625207	hg19	UCSC Ensembl

Cytoband

7q11.22

Allele length

Assembly	Allele length
hg38	5199
hg19	5199

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv12829397, essv12829388, essv12829401, essv12829386, essv12829400, essv12829394, essv12829377, essv12829370, essv12829411, essv12829385, essv12829389, essv12829378, essv12829380, essv12829398, essv12829384, essv12829371, essv12829373, essv12829376, essv12829374, essv12829404, essv12829413, essv12829410, essv12829369, essv12829403, essv12829409, essv12829381, essv12829414, essv12829379, essv12829402, essv12829390, essv12829382, essv12829408, essv12829392, essv12829395, essv12829372, essv12829399, essv12829396, essv12829367, essv12829368, essv12829387, essv12829407, essv12829405, essv12829391, essv12829412, essv12829375, essv12829406, essv12829383, essv12829393

Samples

HG02574, HG03559, HG01098, NA19703, HG02481, NA20274, HG02012, NA19819, HG03190, HG03069, HG03464, HG01325, HG02485, NA19198, HG02595, HG03578, HG03479, HG03224, HG03040, NA19922, HG03212, NA18520, HG02427, HG02545, HG03048, NA19908, HG03088, HG03457, NA19982, HG02887, HG03563, HG03382, HG02817, NA19099, HG02635, HG03064, NA19017, HG02330, NA19712, HG03458, NA19144, HG03259, HG03433, NA19310, HG02676, HG03445, HG02861, HG02760

Known Genes

WBSCR17

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3613620

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	48
Observed Complex	0
Frequency	n/a