Variant Details

Variant: esv3609721

Internal ID

6996641

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr6:80797228..80804073	hg38	UCSC Ensembl
	chr6:81506945..81513790	hg19	UCSC Ensembl

Cytoband

6q14.1

Allele length

Assembly	Allele length
hg38	6846
hg19	6846

Variant Type

CNV loss

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv12450817, essv12450805, essv12450823, essv12450839, essv12450848, essv12450826, essv12450853, essv12450858, essv12450837, essv12450852, essv12450846, essv12450845, essv12450833, essv12450850, essv12450841, essv12450834, essv12450806, essv12450836, essv12450828, essv12450810, essv12450832, essv12450809, essv12450842, essv12450808, essv12450854, essv12450829, essv12450822, essv12450851, essv12450819, essv12450825, essv12450843, essv12450844, essv12450812, essv12450838, essv12450816, essv12450830, essv12450855, essv12450820, essv12450824, essv12450807, essv12450814, essv12450856, essv12450827, essv12450835, essv12450847, essv12450811, essv12450815, essv12450857, essv12450831, essv12450818, essv12450849, essv12450821, essv12450840, essv12450813

Samples

HG01985, HG03484, HG02628, HG03548, NA19399, NA19704, HG02318, HG03300, HG03558, NA19350, HG02476, HG03295, HG03515, HG03139, NA19098, HG02185, NA19448, HG02756, HG02620, HG02549, NA20287, HG02111, HG02178, HG03380, HG02946, NA19239, NA18908, HG03114, HG02442, HG02322, NA18915, HG03428, HG02470, HG03563, HG03472, NA20299, HG03446, HG02635, HG01896, NA19108, NA19256, NA20276, HG03469, NA19467, HG03108, HG02771, HG03097, HG03066, HG03351, HG03401, HG01914, NA19430, HG03072, HG02805

Known Genes

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3609721

Frequency

Sample Size	2504
Observed Gain	0
Observed Loss	54
Observed Complex	0
Frequency	n/a