Variant Details

Variant: esv2671053

Internal ID

9937158

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr9:32711215..32729831	hg38	UCSC Ensembl
Outer	chr9:32711175..32729892	hg38	UCSC Ensembl
Inner	chr9:32711213..32729829	hg19	UCSC Ensembl
Outer	chr9:32711173..32729890	hg19	UCSC Ensembl

Cytoband

9p21.1

Allele length

Assembly	Allele length
hg38	18718
hg19	18718

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

dgv1334e199

Supporting Variants

essv5763721, essv5763121, essv5405029, essv5490070, essv6496263, essv6318362, essv6070179, essv6595377, essv5918372, essv5472868, essv5873982, essv5455044, essv5877784, essv5511346, essv5401077, essv6560405, essv5582059, essv6139118, essv6595586, essv5515177, essv5806432, essv6497018, essv6584267, essv5669926, essv6489952, essv5827212, essv6583583, essv5776793, essv5841319, essv6390387, essv5715062, essv6598227, essv5620082, essv6503064, essv5398265, essv6358560, essv6122369, essv5667162, essv6199329, essv6091917, essv5851268, essv6226579, essv6389069, essv5473404, essv5921589, essv5923089, essv5971618, essv6208211, essv5835639, essv5601975, essv6555375, essv6516514, essv5739222, essv5576300, essv6332392, essv5451563, essv6236001, essv5856644, essv6500818, essv5709030, essv6405925, essv6435006, essv5441074, essv6112742, essv5741010, essv6076551, essv5628415, essv5881893, essv6076634, essv6327381, essv5952953, essv6508607, essv6085337, essv6327563, essv6144629, essv6010740, essv5663678, essv6515782

Samples

NA19701, HG01173, HG00231, NA19397, NA19664, HG01359, NA19734, HG01066, HG00233, NA18528, NA19359, HG01465, NA20294, NA20332, HG00179, HG00150, HG01140, HG00693, HG00641, HG00272, HG00458, HG01492, NA19088, NA19782, HG00185, NA19079, HG01134, HG01455, NA20518, NA20278, NA18977, NA19371, NA19087, HG00182, HG01198, HG00637, HG01048, HG00739, HG00149, NA20800, HG00183, HG01187, HG01515, HG00320, HG01345, HG00635, HG01047, HG00324, NA20299, NA18626, HG00404, HG01383, HG01101, NA18553, NA20296, HG00265, NA19749, HG00565, NA19732, NA12272, HG01253, HG00734, NA18941, NA19010, HG00098, HG01137, HG00116, NA20281, NA19085, HG00578, HG01491, NA19438, NA19223, HG01251, HG01378, HG01111, NA19063, HG00180

Known Genes

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2671053

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	78
Observed Complex	0
Frequency	n/a