Variant Details

Variant: esv2666212

Internal ID

9932317

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr6:80485305..80485399	hg38	UCSC Ensembl
Outer	chr6:80485028..80485675	hg38	UCSC Ensembl
Inner	chr6:81195116..81195022	hg19	UCSC Ensembl
Outer	chr6:81194745..81195392	hg19	UCSC Ensembl

Cytoband

6q14.1

Allele length

Assembly	Allele length
hg38	648
hg19	648

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv5551797, essv6330156, essv6147098, essv6136432, essv5759518, essv6510390, essv6187830, essv5505735, essv6272661, essv5985891, essv5598945, essv6447689, essv5530200, essv6459970, essv6135903, essv6206789, essv6342570, essv5408295, essv5517907, essv5480198, essv6312593, essv6087789, essv5679989, essv5746298, essv5686109, essv6313492, essv5979361, essv5904189, essv5549478, essv5813147, essv5870710, essv6143407, essv5525616, essv5673506, essv6499864, essv6076463, essv5738760, essv6513265, essv6171837, essv5760714, essv5550556, essv5970256, essv6019020, essv6112975, essv6018630, essv5848995, essv6036020, essv5878188, essv5792863, essv5587017, essv6055050, essv5842917, essv5443908, essv6449627, essv5545464, essv5452734, essv6147120, essv5911717, essv6553107, essv5456109, essv5771963, essv5490519, essv5534530, essv6539655, essv6028568, essv6178384, essv5849964, essv6272379, essv5404824, essv5487561, essv5803381, essv5776218, essv6411150, essv6059991, essv5977137, essv5703652, essv5677639, essv6362436, essv5483320, essv5531637, essv5611807, essv5613318, essv6338769, essv6471050, essv6253240, essv5889535, essv5680982, essv6524736, essv5823819, essv6477339, essv6362576, essv6470539, essv6448830, essv5949588, essv6476773, essv5604188

Samples

HG00626, HG00403, NA19701, NA19700, NA19703, HG00231, NA19909, NA19914, NA18980, NA19704, NA20294, NA19355, NA19819, HG00566, NA20332, NA19377, NA20507, NA20356, NA19396, NA19373, HG01350, NA19319, NA19916, HG00270, NA20287, NA19904, NA20291, HG01110, HG00277, HG01069, NA20278, HG00683, HG00335, HG01170, NA18868, NA19917, HG01440, NA19901, HG01048, NA20342, NA19445, NA20127, NA19985, NA19921, NA19007, NA19908, NA19707, NA19403, NA19077, NA12003, HG00653, NA19391, NA19455, NA20314, NA19982, HG00344, NA18637, NA20126, NA18910, HG00740, HG01047, HG01073, NA18856, NA20282, HG00276, NA19452, HG00126, HG01107, NA20296, NA19401, NA19440, NA19390, NA19834, NA20276, NA19712, NA07051, HG01357, HG00607, NA19311, HG00319, NA19360, NA20341, NA19818, HG00111, NA20348, NA19713, NA20289, NA19102, NA19116, NA19711, NA18552, NA19900, NA19430, HG01082, NA20322, HG01437

Known Genes

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2666212

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	96
Observed Complex	0
Frequency	n/a