Variant Details

Variant: esv2676032

Internal ID

9942137

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
	chr5:170702730..170704201	hg38	UCSC Ensembl
	chr5:170129734..170131205	hg19	UCSC Ensembl

Cytoband

5q35.1

Allele length

Assembly	Allele length
hg38	1472
hg19	1472

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

dgv1056e199

Supporting Variants

essv6243544, essv6018330, essv6462956, essv6033420, essv5477835, essv6334396, essv6402847, essv5567042, essv6181572, essv5570742, essv5582386, essv6293504, essv5836291, essv5878250, essv5946477, essv5795254, essv6140223, essv6445066, essv5650044, essv6095262, essv6416918, essv6590226, essv5956907, essv6301438, essv5769154, essv6520123, essv5864927, essv5619373, essv6337188, essv5657100, essv5736330, essv5461118, essv6593121, essv5806373, essv6435323, essv5937754, essv5754394, essv5427675, essv5536583, essv6359018, essv5517368, essv6017201, essv6466867, essv5910148, essv5516357, essv5771115, essv6104899, essv5440151, essv6582902, essv6327733, essv6102763, essv5732997, essv5435926, essv5418275, essv6052897, essv5463645, essv5829970, essv6148241, essv6389187, essv6086995, essv6500461, essv6397360, essv5851234, essv5466623, essv5397418, essv6009383, essv5651809, essv6376335, essv5943046, essv5786462, essv5518806, essv6319077, essv6040178, essv5625571, essv5895726, essv5614464, essv6497438, essv5446340, essv6029241, essv5529441, essv5771498, essv6301391, essv5848844, essv5758007, essv5934789, essv6461152, essv6269440, essv5479662, essv6292831, essv5897183, essv5955474, essv6224990, essv5683583, essv6426427, essv5587976, essv6425948

Samples

HG01441, NA18924, NA19204, HG01359, NA18507, NA18917, NA18486, NA19777, NA18504, HG01456, HG01461, NA19190, NA19098, HG01140, NA19746, NA19171, HG01366, NA19762, NA19728, HG01351, NA19723, NA18923, NA19198, NA19197, NA19771, NA19138, NA18498, NA19681, HG01455, NA19720, NA19651, HG01495, NA19719, NA19137, NA19731, NA19235, NA19172, NA19722, NA19189, NA19209, NA18867, NA19789, HG01136, NA19247, NA19657, NA18934, HG01384, NA19717, NA19663, NA19788, NA18910, NA18871, HG01149, NA19776, NA18907, NA19774, NA19655, NA18856, NA18912, NA18853, NA19682, NA19225, NA19729, NA19652, NA19256, NA18517, NA19749, NA19747, NA19732, HG01551, HG01357, HG01494, HG01113, NA19783, HG01489, HG01342, NA19759, NA19785, NA19779, NA19102, NA18873, NA19770, NA19726, NA19116, NA19780, NA19213, HG01251, NA18505, NA19129, HG01378, NA19755, NA19758, HG01125, NA18511, HG01437, NA19676

Known Genes

KCNIP1

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2676032

Frequency

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