Variant Details

Variant: esv2663062

Internal ID

9582481

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr7:155802622..155815928	hg38	UCSC Ensembl
Outer	chr7:155802251..155816298	hg38	UCSC Ensembl
Inner	chr7:155595316..155608622	hg19	UCSC Ensembl
Outer	chr7:155594945..155608992	hg19	UCSC Ensembl

Cytoband

7q36.3

Allele length

Assembly	Allele length
hg38	14048
hg19	14048

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv5740812, essv5580872, essv5781028, essv5844632, essv6489126, essv6261530, essv5943960, essv5493244, essv6477702, essv5400478, essv6019480, essv6496444, essv5788685, essv5660014, essv5530479, essv6533217, essv5506176, essv5941723, essv5710063, essv5906910, essv6027336, essv5851131, essv5514690, essv6155638, essv6069215, essv5860235, essv5868466, essv5402442, essv5511052, essv5523287, essv5397101, essv6095056, essv5494377, essv6311257, essv6459515, essv6016565, essv6204521, essv6291431, essv6386713, essv5566249, essv6584788, essv5927792, essv6205181, essv5588729, essv6070138, essv5979289, essv5660241, essv5899722, essv6026214, essv6505792, essv6586369, essv5576785

Samples

HG00626, HG00403, HG00650, HG00542, HG00536, HG00671, HG00699, HG00449, HG00654, HG00501, HG00689, HG00448, HG00634, HG00610, HG00537, HG00512, HG00683, HG00534, HG00422, HG00427, HG00530, HG00419, HG00543, HG00629, HG00596, HG00428, HG00701, HG00475, HG00556, HG00533, HG00583, HG00500, HG00708, HG00651, HG00690, HG00404, HG00531, HG00613, HG00525, HG00611, HG00625, HG00418, HG00620, HG00707, HG00672, HG00513, HG00578, HG00421, HG00656, HG00698, HG00595, HG00472

Known Genes

SHH

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)

esv2663062

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	52
Observed Complex	0
Frequency	n/a