Variant Details

Variant: esv2668088

Internal ID

9934193

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr16:88237137..88237383	hg38	UCSC Ensembl
Outer	chr16:88237100..88237433	hg38	UCSC Ensembl
Inner	chr16:88270743..88270989	hg19	UCSC Ensembl
Outer	chr16:88270706..88271039	hg19	UCSC Ensembl

Cytoband

16q24.2

Allele length

Assembly	Allele length
hg38	334
hg19	334

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

Supporting Variants

essv6521218, essv5947656, essv6428353, essv6222817, essv5414406, essv5681537, essv5641402, essv6234746, essv6005241, essv5694516, essv5420823, essv6248269, essv5778083, essv5845492, essv6373853, essv5977359, essv5813360, essv5625816, essv5746684, essv5680071, essv5587550, essv6017882, essv6015592, essv6315007, essv5880650, essv5648837, essv6475154, essv6237057, essv6186569, essv6078879, essv6029123, essv6466526, essv6062133, essv5663211, essv6503277, essv5617783, essv5879973, essv5413511, essv5500997, essv6543206, essv6574222, essv5791540, essv5968914, essv6475066, essv5458222, essv6296658, essv6225818, essv5886839, essv5978673, essv6167509, essv5718177, essv5989550, essv5685810, essv5573663, essv6418448, essv6123350, essv5993774, essv5658259, essv5706452, essv5571521, essv6074425, essv5474879, essv5585421, essv5676623, essv6290258, essv5469329, essv5553070, essv6215563, essv5764689, essv5532771, essv6020387, essv5708272, essv6092745, essv6421764, essv5581136, essv5549902, essv5601938, essv5439384, essv6151207, essv5785138, essv6445309, essv6367972, essv5971882, essv6570374, essv5822365, essv5840423, essv5481864, essv6202420, essv6349024, essv6464182, essv6355279, essv6325361, essv6275362, essv6573814, essv5533466, essv6057083

Samples

NA19394, HG01060, HG01441, HG00650, HG00542, HG00442, HG01173, HG01356, NA19397, HG00608, NA18621, HG00249, HG00524, HG01079, HG01188, HG01066, HG00318, NA19819, NA18530, HG00150, HG00693, HG00138, NA19373, NA19076, NA18550, HG01366, HG01070, HG00501, HG01488, HG00702, HG00689, NA18635, HG01492, NA19130, HG00590, HG01069, HG01067, NA19383, HG00683, HG00106, HG01170, HG01048, HG01133, HG00464, NA19007, HG00313, HG00137, HG01136, NA18613, HG01171, NA19707, HG00328, HG00428, HG00653, NA19391, HG00436, HG00500, NA18910, NA18534, HG00708, HG00692, HG01390, HG01047, HG00651, HG00690, HG00331, HG01101, HG01334, HG00276, HG00463, NA19395, HG01107, HG01204, NA18546, HG00476, HG00580, HG00278, HG01174, HG01375, HG00607, HG00319, HG00418, NA18615, HG00620, NA19398, HG00672, HG00614, HG00421, HG00656, HG00342, HG00698, HG00343, HG01377, HG00628, HG00581, NA18620

Known Genes

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2668088

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	96
Observed Complex	0
Frequency	n/a