Variant Details

Variant: esv2656900

Internal ID

9923005

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chrX:151911344..151920550	hg38	UCSC Ensembl
Outer	chrX:151910973..151920920	hg38	UCSC Ensembl
Inner	chrX:151079816..151089022	hg19	UCSC Ensembl
Outer	chrX:151079445..151089392	hg19	UCSC Ensembl

Cytoband

Xq28

Allele length

Assembly	Allele length
hg38	9948
hg19	9948

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv5631162, essv6262923, essv5431992, essv6275612, essv5733341, essv6474486, essv6359055, essv6005743, essv5536827, essv6576936, essv6397106, essv5871467, essv6297261, essv6516706, essv6122517, essv5659560, essv5730498, essv6542437, essv6292017, essv5477753, essv5539713, essv6033635, essv5727652, essv6368727, essv6060170, essv6372995, essv5744929, essv6574612, essv5698096, essv5428699, essv5851179, essv5969561, essv5551865, essv6346055, essv5967776, essv5952955, essv5517179, essv6424328, essv5487864, essv6398200, essv5674528, essv6343064, essv6296328, essv6454664, essv6018540, essv6267076, essv5613965, essv6430134, essv5767058, essv6399068, essv6082298

Samples

HG01441, HG01356, HG01462, HG01359, HG01389, HG01374, HG01465, HG01456, HG01461, HG01140, HG01250, HG01350, HG01366, HG01351, HG01488, HG01492, HG01354, HG01365, HG01134, HG01455, HG01495, HG01440, HG01550, HG01124, HG01353, HG01136, HG01360, HG01384, HG01498, HG01149, HG01390, HG01383, HG01497, HG01148, HG01551, HG01253, HG01357, HG01375, HG01494, HG01113, HG01137, HG01489, HG01342, HG01491, HG01254, HG01251, HG01377, HG01378, HG01125, HG01112, HG01437

Known Genes

MAGEA4

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2656900

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	51
Observed Complex	0
Frequency	n/a