Variant Details

Variant: esv2664117

Internal ID

9930222

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr1:1605724..1606067	hg38	UCSC Ensembl
Outer	chr1:1605567..1606220	hg38	UCSC Ensembl
Inner	chr1:1541104..1541447	hg19	UCSC Ensembl
Outer	chr1:1540947..1541600	hg19	UCSC Ensembl

Cytoband

1p36.33

Allele length

Assembly	Allele length
hg38	654
hg19	654

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv5517798, essv5527257, essv5826421, essv6488100, essv5717982, essv5828149, essv6246700, essv5979406, essv6574638, essv6453826, essv5918885, essv6301888, essv5691331, essv5449664, essv5401529, essv5998151, essv5415315, essv6222802, essv5732358, essv6261630, essv5842142, essv6301960, essv6139546, essv6205041, essv5530409, essv6200524, essv5464342, essv5732359, essv5451145, essv5984908, essv5792790, essv6205705, essv6285256, essv6532687, essv5766633, essv5498105, essv6215815, essv6084310, essv5931089, essv5622631, essv6316405, essv5671411, essv5409593, essv6255187, essv5966263, essv5565288, essv5526959, essv5624349, essv5923859, essv6282969, essv5661906, essv6407996, essv5872095

Samples

HG01441, NA11830, HG01521, NA11829, HG00187, HG00100, NA11933, HG00640, HG00737, NA19443, NA18519, HG01070, HG00251, NA20769, HG01365, NA11930, NA20539, HG01069, HG00232, NA20340, HG00160, HG00118, HG01133, NA12748, NA20800, HG00268, HG01095, HG01515, HG00436, HG00320, HG00344, NA18637, NA20344, HG01390, HG01073, HG01101, HG00613, NA18593, HG01107, NA12043, NA19434, HG00734, NA20530, NA20516, NA12347, HG00269, HG00312, HG00329, NA18987, HG00310, HG00131, HG00372, HG01125

Known Genes

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2664117

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	53
Observed Complex	0
Frequency	n/a