Variant Details

Variant: esv3588918

Internal ID

6976334

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr1:221205774..221209165	hg38	UCSC Ensembl
Inner	chr1:221205775..221209165	hg38	UCSC Ensembl
Outer	chr1:221205774..221209166	hg38	UCSC Ensembl
	chr1:221379116..221382507	hg19	UCSC Ensembl
Inner	chr1:221379117..221382507	hg19	UCSC Ensembl
Outer	chr1:221379116..221382508	hg19	UCSC Ensembl

Cytoband

1q41

Allele length

Assembly	Allele length
hg38	3392
hg19	3392

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv10299711, essv10299714, essv10299719, essv10299677, essv10299720, essv10299712, essv10299684, essv10299697, essv10299678, essv10299699, essv10299689, essv10299717, essv10299713, essv10299705, essv10299690, essv10299681, essv10299702, essv10299695, essv10299683, essv10299709, essv10299718, essv10299679, essv10299708, essv10299680, essv10299703, essv10299688, essv10299687, essv10299701, essv10299716, essv10299676, essv10299698, essv10299686, essv10299706, essv10299700, essv10299704, essv10299715, essv10299692, essv10299685, essv10299694, essv10299696, essv10299707, essv10299693, essv10299682, essv10299691, essv10299710

Samples

HG01079, HG01188, HG00367, HG01486, HG00177, NA12399, HG01682, NA19764, NA19678, HG03490, HG01083, NA21108, NA20539, HG00120, HG00232, NA20869, NA21129, HG01133, HG01058, HG00253, NA20515, HG01136, HG01171, HG01684, NA20810, NA20760, NA20525, HG01512, NA20903, HG01197, HG00321, HG01700, HG01530, HG03934, NA19729, HG02223, HG01174, HG01205, NA21125, NA20906, NA20334, NA19716, HG01055, HG00131, HG03886

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3588918

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	45
Observed Complex	0
Frequency	n/a