Variant Details

Variant: esv2659146

Internal ID

9578565

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chrX:155560528..155573651	hg38	UCSC Ensembl
	chrX:154790189..154803312	hg19	UCSC Ensembl

Cytoband

Xq28

Allele length

Assembly	Allele length
hg38	13124
hg19	13124

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv6171527, essv6437778, essv5893322, essv5585872, essv6439648, essv6486058, essv5432850, essv5526758, essv6500757, essv5612682, essv6558862, essv6055151, essv5586638, essv5458868, essv5777822, essv5516559, essv6401501, essv5700070, essv6583965, essv5470761, essv5659914, essv5771351, essv5456348, essv6349823, essv5925000, essv6283919, essv6047513, essv5546994, essv5767147, essv5871800, essv6275735, essv5701368, essv6264636, essv6243840, essv5588427, essv5790377, essv5913239, essv5696202, essv5408437, essv5775132, essv6329259, essv5673563, essv5748309, essv6199916, essv6013129, essv6250976, essv6202311, essv6395145, essv5705094, essv5922991, essv5567591, essv6020772, essv6056450, essv5802508, essv5603884, essv5919400, essv6205658, essv5696849, essv5681201, essv6292958, essv5727212, essv6155328, essv6517380, essv6234387, essv6127292, essv6435753, essv5534846, essv5792178, essv6491046, essv6181115, essv5626314, essv6422751, essv6204258, essv5621695, essv5778034, essv6463152, essv6015032, essv6566773, essv5912597, essv6017955, essv6498353, essv5712276, essv5547708, essv5875113, essv6073298, essv6535559, essv5484788, essv6142803, essv6204856, essv6359993, essv5796387, essv6120666, essv6082806, essv5881570, essv6067343, essv6582600, essv5839117, essv5399417, essv5553322, essv6435293, essv6349931, essv6245480, essv5646334, essv6126787, essv6205771, essv6166889, essv5857328, essv5635125, essv5823681

Samples

HG00309, HG01515, NA12718, HG00313, HG01518, HG00252, HG00536, HG00182, HG00344, HG01353, HG01072, HG01519, HG00328, HG00500, HG01173, HG00171, HG00463, HG00657, HG00189, HG00375, HG01174, HG00270, HG01350, HG00139, HG00683, HG00334, HG00404, HG00557, HG01134, NA19682, HG00177, HG00331, NA19780, HG01171, NA18626, HG00479, NA18628, HG00554, HG01521, HG00342, HG00154, HG00242, NA19085, HG00346, HG00179, HG00250, HG01140, HG00583, HG00337, NA19675, NA18623, HG00610, HG01061, HG00231, HG00689, NA12273, HG00330, HG00338, HG00178, HG00125, HG00258, HG01136, HG00174, HG00357, NA20589, HG00237, HG00343, HG00584, HG00306, HG00620, HG01516, HG00185, HG00559, HG00176, HG00560, HG00265, HG00282, HG00249, NA20818, HG00277, HG00513, HG00524, HG00329, HG00525, HG01060, HG00589, HG01149, HG01137, HG00595, NA19078, HG00118, HG00448, NA18602, NA20509, HG00281, HG00285, HG00422, HG00693, HG00566, HG01125, HG00251, HG00275, HG00324, HG00625, HG00690, HG01522, HG00671, HG00702, HG00327

Known Genes

TMLHE

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

High quality site

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2659146

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	109
Observed Complex	0
Frequency	n/a