Variant Details

Variant: esv2657024

Internal ID

9923129

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr10:73363920..73368038	hg38	UCSC Ensembl
	chr10:75123678..75127796	hg19	UCSC Ensembl

Cytoband

10q22.2

Allele length

Assembly	Allele length
hg38	4119
hg19	4119

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv5766539, essv5807783, essv6474420, essv6544671, essv5477970, essv5995164, essv6309275, essv5991606, essv5791128, essv5473520, essv5492343, essv6180235, essv5488322, essv5704769, essv6003480, essv6482173, essv5417121, essv5504820, essv6274534, essv5950429, essv6262960, essv5845437, essv6416250, essv5702715, essv5796142, essv5601574, essv5460303, essv5730049, essv5491542, essv5559569, essv5736152, essv5684184, essv6533423, essv5772023, essv6160902, essv6250704, essv6555802, essv6333630, essv5978175, essv6360974, essv6367874, essv5764483, essv5945109, essv5945011, essv5860444, essv6523255, essv6269905, essv5848513, essv5845390, essv6511057, essv5899897, essv6233801, essv5924544, essv5908391, essv5438136, essv5954748, essv6212956, essv6555851

Samples

NA20543, NA19397, NA19909, NA19399, NA19092, NA20294, NA19819, NA19393, NA19920, NA19396, NA19379, NA19382, NA19315, NA19198, NA19916, NA18498, NA20287, NA18874, NA18868, NA19385, NA19722, HG01198, NA19985, NA18867, NA19247, NA19437, NA20787, NA19403, NA18933, NA18871, HG01047, NA18856, NA19682, HG01204, NA19401, NA19375, NA19390, NA19834, NA19256, NA20276, NA19473, NA19835, NA20792, HG00237, NA19428, NA19360, NA20341, NA19398, NA19248, NA19438, NA19472, NA20334, NA19102, NA19213, HG01082, NA19316, NA20322, NA18487

Known Genes

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)

esv2657024

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	58
Observed Complex	0
Frequency	n/a