Variant Details

Variant: esv2667912

Internal ID

9934017

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr15:23746939..23750791	hg38	UCSC Ensembl
	chr15:23992086..23995938	hg19	UCSC Ensembl

Cytoband

15q11.2

Allele length

Assembly	Allele length
hg38	3853
hg19	3853

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv6386392, essv6246971, essv5846790, essv5473810, essv6397249, essv6536814, essv5890466, essv6551282, essv6213036, essv5876518, essv5738906, essv5415179, essv6529504, essv5908357, essv5870926, essv6166502, essv5627188, essv5569797, essv6317085, essv5740625, essv5649088, essv5555393, essv6156107, essv6280793, essv5596442, essv6437978, essv5578598, essv5564594, essv6012531, essv5400052, essv6302908, essv5706609, essv6210115, essv6430343, essv6597089, essv6080965, essv5501332, essv5736478, essv6357226, essv6384366, essv5792490, essv5456484, essv6106737, essv5561579, essv5690205, essv5396333, essv5959700, essv5891374, essv6540536, essv6189487, essv6392869, essv6186362, essv5448733, essv6002792, essv5961659, essv5875970

Samples

HG01060, NA18621, NA18861, HG01066, NA20512, NA18486, NA19393, NA18530, NA18616, NA19107, NA19448, HG01167, NA19723, NA18942, NA18574, NA18571, NA19138, NA18964, HG00590, NA18560, NA18617, NA19172, HG00422, NA18986, HG00427, NA18908, NA19789, NA18614, NA20524, HG00533, HG00583, NA19081, NA18572, NA18630, NA18548, NA19000, HG00479, NA18499, NA18523, NA18858, NA18634, NA18576, NA19834, HG00580, HG01375, NA20792, NA19470, NA19398, NA19472, NA20826, NA19711, NA18983, NA20502, NA19129, NA19346, NA19074

Known Genes

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

High quality site

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2667912

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	56
Observed Complex	0
Frequency	n/a