Variant Details

Variant: esv2666858

Internal ID

9932963

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr17:33470837..33471009	hg38	UCSC Ensembl
	chr17:31797855..31798027	hg19	UCSC Ensembl

Cytoband

17q11.2

Allele length

Assembly	Allele length
hg38	173
hg19	173

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv5683758, essv6409702, essv6556151, essv6406154, essv6358038, essv6544037, essv6525131, essv6137612, essv6226880, essv5940624, essv6065583, essv5558798, essv6467043, essv6030745, essv6535484, essv6226202, essv6381953, essv5411748, essv5422595, essv5594162, essv5548694, essv5910033, essv6311854, essv6343851, essv6096967, essv6122549, essv6186212, essv5730060, essv6508251, essv5711512, essv6391898, essv5883267, essv6117362, essv6444891, essv6128963, essv5692755, essv6492784, essv6550953, essv5792384, essv6431927, essv6467614, essv5928576, essv5968665, essv6458699, essv5984663, essv5842742, essv5419164, essv6206320, essv6134298, essv6036853, essv5585437, essv6360800, essv5397172, essv6032313, essv5600606, essv5514443, essv5415272

Samples

HG00626, NA19394, NA18502, HG00608, NA11931, NA20813, NA12045, NA19359, NA18486, NA12004, NA18510, NA19446, NA07346, NA19379, NA18944, NA19382, HG00173, HG00590, NA20811, HG00530, NA20515, NA19210, NA18613, NA19077, NA19391, NA19236, NA19982, NA18566, NA18573, NA19461, NA18499, NA11894, NA12249, HG01101, NA18853, NA19395, NA20542, NA18945, NA19401, NA11881, NA18952, NA19434, NA19473, NA20815, NA19380, NA19360, NA18615, NA12749, NA19093, NA19430, NA19129, NA12890, NA18511, NA19346, NA18562, NA18577, NA20772

Known Genes

ASIC2

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2666858

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	57
Observed Complex	0
Frequency	n/a