Variant Details

Variant: esv2664857

Internal ID

9930962

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr7:100673293..100676299	hg38	UCSC Ensembl
Outer	chr7:100672922..100676669	hg38	UCSC Ensembl
Inner	chr7:100270916..100273922	hg19	UCSC Ensembl
Outer	chr7:100270545..100274292	hg19	UCSC Ensembl

Cytoband

7q22.1

Allele length

Assembly	Allele length
hg38	3748
hg19	3748

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv6137735, essv6136442, essv5827129, essv6301230, essv6315780, essv5955383, essv6144193, essv5795618, essv6407439, essv6240341, essv6291391, essv6082496, essv6119909, essv5894764, essv5781434, essv5854222, essv6202956, essv5457497, essv5991062, essv6214033, essv6595778, essv5825083, essv5609448, essv5623166, essv5706487, essv5681028, essv5621500, essv5729014, essv5478584, essv5601008, essv6314951, essv5532561, essv6349268, essv6509261, essv6087804, essv5820246, essv6248159, essv6576741, essv5551321, essv6110637, essv6118471, essv5579204, essv5509389, essv5844608, essv6501290, essv6208876, essv5696950, essv5734505, essv5940613, essv5999030, essv6462039, essv6109842

Samples

NA20588, NA20543, NA20766, NA20508, NA20783, NA20514, NA20816, NA20813, NA20532, NA20805, NA20808, NA20507, NA20537, NA20589, NA20768, NA20540, NA20513, NA20541, NA20518, NA20819, NA20812, NA20811, NA20757, NA20515, NA20753, NA20818, NA20535, NA20505, NA20809, NA20536, NA20770, NA20525, NA20538, NA20828, NA20542, NA20534, NA20765, NA20522, NA20801, NA20804, NA20785, NA20527, NA20778, NA20504, NA20582, NA20510, NA20826, NA20503, NA20502, NA20585, NA20754, NA20509

Known Genes

GNB2

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)

esv2664857

Frequency

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