Variant Details

Variant: esv3622805

Internal ID

6662974

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr10:31210018..31211038	hg38	UCSC Ensembl
Inner	chr10:31210025..31211032	hg38	UCSC Ensembl
Outer	chr10:31210012..31211045	hg38	UCSC Ensembl
	chr10:31498947..31499967	hg19	UCSC Ensembl
Inner	chr10:31498954..31499961	hg19	UCSC Ensembl
Outer	chr10:31498941..31499974	hg19	UCSC Ensembl

Cytoband

10p11.22

Allele length

Assembly	Allele length
hg38	1021
hg19	1021

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv13749171, essv13749177, essv13749252, essv13749192, essv13749190, essv13749240, essv13749248, essv13749201, essv13749250, essv13749211, essv13749194, essv13749221, essv13749206, essv13749253, essv13749172, essv13749189, essv13749227, essv13749175, essv13749246, essv13749231, essv13749207, essv13749236, essv13749191, essv13749257, essv13749233, essv13749183, essv13749238, essv13749186, essv13749225, essv13749247, essv13749210, essv13749200, essv13749199, essv13749193, essv13749237, essv13749196, essv13749229, essv13749176, essv13749195, essv13749259, essv13749218, essv13749220, essv13749230, essv13749179, essv13749245, essv13749249, essv13749187, essv13749239, essv13749173, essv13749205, essv13749255, essv13749212, essv13749217, essv13749234, essv13749223, essv13749243, essv13749184, essv13749181, essv13749203, essv13749219, essv13749251, essv13749198, essv13749208, essv13749209, essv13749232, essv13749204, essv13749258, essv13749188, essv13749222, essv13749244, essv13749241, essv13749214, essv13749174, essv13749213, essv13749226, essv13749242, essv13749260, essv13749185, essv13749216, essv13749197, essv13749235, essv13749254, essv13749224, essv13749215, essv13749178, essv13749180, essv13749228, essv13749202, essv13749256, essv13749182

Samples

NA20339, NA19222, HG02628, HG02583, NA19466, NA18508, HG03163, HG02973, HG03175, HG02337, HG03300, HG02836, NA18877, HG02323, HG03280, NA18504, HG02536, HG03436, HG02811, HG02016, HG03135, HG02810, NA19762, HG03499, HG02595, HG03370, HG02854, NA19197, NA19904, HG02505, HG03268, HG02573, HG02634, NA19917, HG02461, HG02427, NA19209, HG03058, HG03394, HG02819, HG03343, HG03160, HG03088, HG03547, NA19913, HG01989, HG01077, HG03027, HG01049, HG03311, HG01102, NA18879, HG03382, HG03078, HG01101, HG03024, HG03046, HG02666, NA20296, HG02813, HG02255, NA19206, HG03028, NA19309, HG03240, NA19147, NA19434, HG03539, HG01915, HG02923, HG02837, NA19380, HG03259, HG02982, HG02839, HG01342, NA19323, HG03432, NA20348, NA19248, HG03049, HG03351, NA19900, HG02947, HG02855, HG03198, HG02629, HG03303, NA19214, HG02760

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3622805

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	90
Observed Complex	0
Frequency	n/a