Variant Details

Variant: esv2675318

Internal ID

9941423

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr1:110471109..110472270	hg38	UCSC Ensembl
	chr1:111013731..111014892	hg19	UCSC Ensembl

Cytoband

1p13.3

Allele length

Assembly	Allele length
hg38	1162
hg19	1162

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv6065982, essv6382909, essv6272961, essv6294187, essv6264791, essv6010419, essv5500502, essv5500768, essv5401250, essv5827414, essv5996962, essv6111002, essv6525103, essv6407110, essv6117489, essv6181051, essv6370391, essv6055453, essv5464664, essv6072148, essv5554416, essv5460859, essv6349216, essv6593483, essv6454386, essv5494535, essv6015170, essv5649258, essv6202354, essv5907358, essv5730430, essv5659205, essv5866819, essv5609763, essv6091540, essv6141138, essv5662301, essv6117220, essv5449339, essv6068043, essv6484055, essv6430545, essv6279480, essv5517354, essv6175814, essv5497900, essv6255155, essv6038902, essv5824936, essv6204645, essv5826396, essv5916416, essv6126813, essv5902698, essv6354489, essv6332190

Samples

HG00626, HG00442, HG00671, HG00654, HG00693, HG00663, HG00501, HG00702, HG00689, HG00448, HG00634, HG00537, HG00590, HG00683, HG00534, HG00705, HG00427, HG00530, HG00464, HG00543, HG00560, HG00443, HG00596, HG00557, HG00428, HG00653, HG00577, HG00701, HG00475, HG00583, HG00708, HG00692, HG00651, HG00690, HG00479, HG00613, HG00525, NA18963, HG00704, HG00463, HG00611, HG00476, HG00580, HG00473, HG00607, HG00662, HG00418, HG00707, HG00672, HG00478, HG00656, HG00698, HG00472, HG00628, HG00437, HG00581

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)

esv2675318

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	56
Observed Complex	0
Frequency	n/a