Variant Details

Variant: esv3635780

Internal ID

7022578

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr15:22095526..22146218	hg38	UCSC Ensembl
	chr15:22383477..22434169	hg19	UCSC Ensembl

Cytoband

15q11.2

Allele length

Assembly	Allele length
hg38	50693
hg19	50693

Variant Type

CNV gain

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

dgv437e214

Supporting Variants

essv15163867, essv15163906, essv15163896, essv15163885, essv15163872, essv15163886, essv15163897, essv15163882, essv15163887, essv15163889, essv15163874, essv15163892, essv15163904, essv15163883, essv15163884, essv15163908, essv15163871, essv15163913, essv15163873, essv15163898, essv15163877, essv15163890, essv15163865, essv15163893, essv15163879, essv15163875, essv15163866, essv15163911, essv15163894, essv15163888, essv15163912, essv15163876, essv15163909, essv15163899, essv15163863, essv15163901, essv15163891, essv15163864, essv15163869, essv15163861, essv15163881, essv15163870, essv15163880, essv15163895, essv15163868, essv15163862, essv15163900, essv15163907, essv15163903, essv15163910, essv15163878, essv15163905, essv15163902

Samples

NA18998, NA19701, NA20339, NA18861, NA21100, HG02017, NA21137, HG03782, HG02153, NA18597, NA20890, HG02549, HG03874, NA19197, HG03189, HG01767, NA21107, HG00253, NA18544, HG02439, HG03132, HG02793, HG02322, HG00692, NA20903, HG00331, NA18856, HG03672, NA21142, HG01589, HG01990, HG01811, NA19401, HG00742, HG01598, HG03846, NA07037, NA19818, NA18501, HG03066, HG01846, NA21133, NA20528, HG02052, NA18968, HG04153, NA18740, HG03815, HG03698, HG00180, NA21120, HG00255, HG03741

Known Genes

OR4N3P, OR4N4

Method

Sequencing

Analysis

Platform

Multiple platforms

Comments

Reference

1000_Genomes_Consortium_Phase_3

Pubmed ID

21293372

Accession Number(s)

esv3635780

Frequency

Sample Size	2504
Observed Gain	53
Observed Loss	0
Observed Complex	0
Frequency	n/a