Variant Details

Variant: esv2658675

Internal ID

9924780

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr1:222200324..222207980	hg38	UCSC Ensembl
Outer	chr1:222199953..222208350	hg38	UCSC Ensembl
Inner	chr1:222373666..222381322	hg19	UCSC Ensembl
Outer	chr1:222373295..222381692	hg19	UCSC Ensembl

Cytoband

1q41

Allele length

Assembly	Allele length
hg38	8398
hg19	8398

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

dgv99e199

Supporting Variants

essv6131411, essv5685357, essv5831311, essv6415545, essv5977905, essv5772000, essv5867151, essv5921001, essv5810204, essv5458716, essv5581185, essv6361505, essv5566117, essv5656820, essv5821600, essv6291788, essv5592855, essv5546130, essv5853704, essv6004995, essv6348601, essv5695075, essv6092367, essv6106301, essv5936814, essv5428833, essv5508673, essv6018023, essv5552915, essv6429062, essv5814191, essv6128263, essv5439176, essv6099137, essv5441565, essv5487532, essv6207085, essv6387310, essv6235552, essv5405219

Samples

NA20543, NA20766, NA20508, NA20532, NA20512, NA20771, NA20814, NA20537, NA20756, NA20795, NA20768, NA20541, NA20518, NA20535, NA20787, NA20524, NA20505, NA20809, NA20810, NA20506, NA20519, NA20770, NA20525, NA20538, NA20828, NA20542, NA20801, NA20785, NA20530, NA20527, NA20792, NA20504, NA20797, NA20786, NA20807, NA20758, NA20826, NA20528, NA20754, NA20509

Known Genes

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2658675

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	40
Observed Complex	0
Frequency	n/a