Variant Details

Variant: esv2669017

Internal ID

9935122

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr15:65581273..65581441	hg38	UCSC Ensembl
	chr15:65873611..65873779	hg19	UCSC Ensembl

Cytoband

15q22.31

Allele length

Assembly	Allele length
hg38	169
hg19	169

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv6013058, essv5515407, essv5654098, essv5498819, essv6157858, essv5546619, essv6400680, essv6586883, essv6260146, essv6551406, essv6353693, essv5873207, essv6199111, essv6384047, essv5914722, essv5497389, essv5864126, essv6363894, essv6061248, essv5659837, essv5755202, essv6047770, essv6246094, essv6396631, essv6565505, essv6060652, essv6394133, essv5658373, essv6283024, essv6111519, essv6515434, essv5565866, essv6452790, essv6458138, essv6082325, essv5799984, essv5697450, essv6236460, essv6289661, essv5872418, essv6214520, essv6311815, essv6154832, essv6041167, essv5417800, essv6365108, essv5554015, essv6390573, essv6101732, essv5950574, essv6179755, essv6037931, essv6586747, essv6010937, essv6212318, essv6327151, essv5424481, essv6422533

Samples

HG01462, HG00257, HG01389, HG01374, NA19355, NA20507, HG00271, NA19374, HG00138, NA19381, NA18519, HG01070, NA19762, HG01083, HG00537, NA19404, HG01170, HG00236, NA19371, NA12889, HG01440, HG00427, NA18520, HG00323, HG00253, HG00260, HG00137, NA18544, NA18613, NA19403, NA12003, NA19391, NA19455, HG00436, HG00275, HG01390, HG00479, HG01101, HG00140, HG00704, HG00246, NA18632, NA19390, HG00285, HG00136, HG00278, HG01375, HG00237, NA19360, HG00256, HG00339, HG00111, HG00329, NA20289, HG00186, HG00252, HG01437, NA18620

Known Genes

VWA9

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2669017

Frequency

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