Variant Details

Variant: esv2674977

Internal ID

9941082

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr2:175481388..175487844	hg38	UCSC Ensembl
Outer	chr2:175480817..175488264	hg38	UCSC Ensembl
Inner	chr2:176346116..176352572	hg19	UCSC Ensembl
Outer	chr2:176345545..176352992	hg19	UCSC Ensembl

Cytoband

2q31.1

Allele length

Assembly	Allele length
hg38	7448
hg19	7448

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

dgv748e199

Supporting Variants

essv5895787, essv5719865, essv5622855, essv6414532, essv5748230, essv6293998, essv5706603, essv6032405, essv6294937, essv6139751, essv6229757, essv6147024, essv5609860, essv5657489, essv6199519, essv5833753, essv6574590, essv6218255, essv5549939, essv6450195, essv5776847, essv5518483, essv5776618, essv6061634, essv5522566, essv6491619, essv5521792, essv6177249, essv5967006, essv5925048, essv6512805, essv6587445, essv6467795, essv5780383, essv5542179, essv6227512, essv5913136, essv6109255, essv6325809, essv5594977, essv6506544, essv6310185, essv6079688, essv6373795, essv5496491, essv5588643, essv6548557, essv5402150, essv5647656, essv6036928, essv5910994, essv5720868, essv6332663, essv6215930, essv5433801, essv5988740, essv6227172, essv6491608, essv5942967, essv6108076, essv6543143, essv5463513, essv5552190, essv6313854, essv6432526, essv6311582, essv5584924, essv6334135, essv5662612, essv6077774, essv5512184, essv5602279, essv5918846, essv6318836, essv5536298, essv5817516, essv6500930, essv5643500, essv5674707, essv5779824, essv5727630, essv5495412, essv5957244, essv6040541, essv6446648, essv6445045, essv6040071, essv6263053, essv6195440, essv5962821, essv6111738, essv6148809, essv6519215, essv6408817, essv6185220, essv6300020, essv5659020, essv5850795, essv5828400, essv6055164, essv6162911, essv5891256, essv5881530, essv5792112, essv5694961, essv6068223, essv6560166, essv6520950, essv5809134, essv5695143, essv6004376, essv5549983, essv6522908, essv5967071, essv6384710

Samples

NA18502, NA19058, NA19703, NA18621, NA18861, NA18592, NA18508, NA18565, NA18561, NA19704, NA18599, NA18603, NA18545, NA19819, NA18596, NA19377, NA18530, NA18606, NA19443, NA19190, NA18870, NA18526, NA19920, NA18602, NA18988, NA19374, NA18563, NA18944, NA18940, NA18550, NA18597, NA18595, NA18635, NA18558, NA18916, NA18582, NA18571, NA18498, NA18964, NA19130, NA19079, NA18611, NA19404, NA18868, NA18560, NA19075, NA19172, NA18990, NA18557, NA18985, NA18638, NA19007, NA18614, NA18544, NA18613, NA19056, NA18637, NA18871, NA18572, NA18948, NA18534, NA18548, NA18907, NA18537, NA18573, NA19114, NA18532, NA19099, NA19257, NA18555, NA18536, NA19395, NA18858, NA18634, NA18593, NA18945, NA18541, NA18576, NA18546, NA18608, NA18953, NA19375, NA18632, NA18542, NA18909, NA19108, NA18961, NA18952, NA18543, NA19147, NA18559, NA18517, NA19712, NA18564, NA19380, NA19428, NA19083, NA18610, NA19818, NA18501, NA19093, NA18636, NA18609, NA19080, NA19711, NA18552, NA18984, NA18505, NA19129, NA18511, NA18522, NA18612, NA18549, NA18562, 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)

esv2674977

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	115
Observed Complex	0
Frequency	n/a