Variant Details

Variant: esv2657682

Internal ID

9923787

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr11:18076206..18078565	hg38	UCSC Ensembl
	chr11:18097753..18100112	hg19	UCSC Ensembl

Cytoband

11p15.1

Allele length

Assembly	Allele length
hg38	2360
hg19	2360

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv6311612, essv5481515, essv5414350, essv6308806, essv5661942, essv5785801, essv6485799, essv5725323, essv6072694, essv5608408, essv5789243, essv6074035, essv5438762, essv5726401, essv6439314, essv6260958, essv5599577, essv6200058, essv6285172, essv5979773, essv5585313, essv5846900, essv5874071, essv6275036, essv5433205, essv6353831, essv5421928, essv6459062, essv6264255, essv6540877, essv5703950, essv5857634, essv6511499, essv6246464, essv5715966, essv6090750, essv6587997, essv6525635, essv6276323, essv6141149, essv6161779, essv6487247, essv6222303, essv6342962, essv5605158, essv5582605, essv5759377, essv6109532, essv5544045, essv5597478, essv5682289, essv5964347, essv6166917, essv5648327, essv5508984, essv5883664

Samples

HG01060, HG01173, HG01079, HG00100, NA20813, HG01456, NA12399, HG01140, NA20814, HG01488, HG00736, NA19904, HG00139, NA12282, NA19651, HG01067, NA20518, NA06984, HG00236, HG00262, HG01176, HG00182, NA19725, HG01198, NA20757, NA20533, NA20818, HG01353, HG00313, HG00188, HG00176, HG00282, NA19663, HG00324, HG00373, NA12829, HG01497, HG01334, HG00265, HG00357, HG00136, NA20790, NA20778, HG00116, HG01489, HG01491, NA12749, NA19716, HG00174, HG00123, HG00186, NA19711, HG00372, NA12154, HG01191, HG00180

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)

esv2657682

Frequency

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