Variant Details

Variant: esv2669106

Internal ID

9935211

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr8:142122684..142122889	hg38	UCSC Ensembl
	chr8:143204045..143204250	hg19	UCSC Ensembl

Cytoband

8q24.3

Allele length

Assembly	Allele length
hg38	206
hg19	206

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv6017872, essv6397263, essv5405911, essv6361423, essv6588360, essv5499757, essv6481155, essv6057486, essv5587399, essv5790856, essv5583355, essv5411200, essv6298039, essv6276808, essv5612193, essv6000807, essv6241897, essv6360867, essv5689327, essv5655668, essv5777323, essv5574257, essv5480528, essv6462565, essv6267756, essv6314185, essv6516716, essv5792109, essv5698991, essv6190103, essv6439754, essv6476924, essv6523619, essv5574694, essv5688476, essv6109061, essv5571502, essv6506739, essv6048258, essv5684419, essv5578102, essv6542326, essv5813724, essv5998811, essv6227400, essv6339908, essv6430354, essv5781416, essv6146331, essv5766538, essv6170815, essv5629415, essv6351749, essv5750731, essv5452215, essv5554896, essv5847606, essv5453556, essv6244670, essv5577100, essv5792073, essv6387708, essv6033865, essv6108695, essv6434384, essv5496989, essv6418672, essv5971934, essv6565506, essv6373989, essv6237972, essv6379488, essv6184306, essv5498855, essv6143455, essv5617516, essv5801736, essv6176860, essv6320382, essv6172383, essv5966629, essv6366504, essv5649457, essv5921142

Samples

NA19700, NA19055, HG01052, NA20813, NA20802, NA19350, HG00699, NA20805, NA19777, NA19443, NA19920, NA18602, NA19107, NA19396, NA19373, NA19005, NA18489, NA19728, HG01488, NA12348, NA07048, NA18582, HG01134, HG00281, NA19075, NA19385, NA19471, NA18985, NA20127, HG00323, NA19985, HG00253, HG00264, NA12777, HG01136, NA20800, NA19657, NA18538, NA20505, NA19077, NA18956, NA20810, HG00320, NA19081, NA19788, NA12718, NA19654, NA20581, HG01383, HG00157, NA18963, NA19625, NA19440, NA19072, NA12272, HG00136, NA18941, NA20804, HG00278, NA19010, NA20530, NA20527, HG00308, NA19439, HG00116, NA19083, NA20797, NA20281, NA18615, HG01342, HG00707, NA19785, HG01254, NA20807, NA11843, NA20758, HG00377, NA18984, NA18989, NA19004, HG01111, HG01191, HG00437, HG01516

Known Genes

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2669106

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	84
Observed Complex	0
Frequency	n/a