Variant Details

Variant: esv2671562

Internal ID

9937667

Landmark

Location Information

Type	Coordinates	Assembly	Other Links
Inner	chr14:35136660..35145966	hg38	UCSC Ensembl
Outer	chr14:35135939..35146436	hg38	UCSC Ensembl
Inner	chr14:35605866..35615172	hg19	UCSC Ensembl
Outer	chr14:35605145..35615642	hg19	UCSC Ensembl

Cytoband

14q13.2

Allele length

Assembly	Allele length
hg38	10498
hg19	10498

Variant Type

CNV deletion

Copy Number

Allele State

Allele Origin

Probe Count

Validation Flag

Merged Status

Merged Variants

dgv390e199

Supporting Variants

essv5854177, essv5906071, essv5399914, essv6061048, essv5403594, essv6418671, essv5704521, essv6591537, essv6224785, essv6000015, essv5469123, essv5635842, essv5885415, essv6570792, essv5876229, essv5424222, essv5431460, essv6376559, essv5861586, essv5726135, essv5687745, essv5505286, essv5605541, essv5628777, essv5414520, essv5409629, essv6315937, essv6008506, essv5479704, essv5695749, essv6014969, essv5601301, essv5639685, essv5777912, essv5480633, essv6256339, essv6052937, essv6490410, essv5547157, essv6415779, essv6297459, essv5934243, essv6493064, essv6325678, essv6042328, essv5706596, essv6014348, essv6233862, essv6594642, essv6067712, essv5954469, essv5836725, essv6423719, essv5791568, essv6358274, essv5744484, essv5781259, essv5917850, essv5733427, essv6247427, essv6300699, essv6492153, essv6475160, essv6586321, essv6319702, essv5964002, essv5800370, essv5579828, essv6383218, essv5749443, essv5553482, essv6437483, essv5694435, essv5649945, essv6328604, essv6169658, essv5837144, essv6145817, essv5513911, essv5983565, essv5760905, essv5892051, essv5818822, essv5526199, essv5496550, essv6357361, essv6179136, essv6294193, essv5878152, essv5488383, essv5960918, essv5713267, essv5776011, essv5802046, essv5419368, essv5670407, essv5608328, essv5841527, essv6160990, essv5943691, essv5598773, essv6538439, essv5457203, essv5405262, essv5896235, essv6040101, essv5519078, essv5802940, essv6546215, essv5974627, essv5427556, essv6324212, essv5768823, essv6356919, essv5395708, essv5927891, essv6390330, essv6509562, essv6424296, essv5829368, essv6218614, essv6116570, essv6219427, essv6498773, essv5883937, essv6361809, essv5796238, essv6011049, essv5494107, essv6108206, essv6564012, essv6286019, essv6442674, essv5988090, essv6098678, essv6469656, essv6152805, essv6342108, essv6195385, essv5683055, essv6295097, essv6089337, essv5901692, essv6083451

Samples

HG00626, HG00442, NA19648, NA19058, HG00592, HG01521, NA19055, HG00536, HG00608, NA18947, NA18980, NA18999, HG00181, HG00699, NA19057, NA18959, HG00449, HG01522, HG00693, NA18988, HG00337, HG00327, HG00663, HG00589, HG00272, NA19728, HG00330, NA19062, HG00346, NA19088, NA19054, HG00270, NA19681, NA18964, HG00590, HG00281, NA19651, HG00335, NA19719, NA19731, HG00534, NA19075, HG00422, HG00705, NA18986, HG00309, NA19722, NA19002, NA18990, NA18975, HG00323, NA18973, HG00419, NA19789, HG00464, NA19007, HG00543, NA18951, HG00560, HG00629, NA19657, HG00443, NA19082, HG00282, NA19070, HG00328, HG00428, HG00577, HG00701, HG00475, HG00436, HG00556, HG00320, HG00584, HG00500, NA18948, HG00619, NA18981, HG00708, HG00692, HG00635, NA19064, HG00273, HG00651, NA19000, NA19655, HG00404, HG00373, HG00331, HG00684, HG00525, NA19059, NA19761, HG00704, HG00463, NA18945, NA19012, NA18974, NA18953, NA19003, HG00611, HG00476, NA18961, NA18952, NA19747, HG00353, NA19072, NA18950, HG00580, NA18941, NA19773, HG00473, HG00607, NA19786, NA19083, NA18943, NA19783, HG00662, HG00418, NA19085, HG00620, HG00339, HG00707, HG00614, HG00513, HG00578, NA18971, HG00421, HG00329, NA19716, HG00698, HG00280, NA19780, HG00595, NA18984, HG00472, NA19004, HG00628, HG00180, NA19074, HG00437, NA18965, HG01516, HG00593

Known Genes

KIAA0391

Method

Merging

Analysis

No reference, merging analysis

Platform

Merging

Comments

Reference

1000_Genomes_Consortium_Phase_1

Pubmed ID

23128226

Accession Number(s)

esv2671562

Frequency

Sample Size	1151
Observed Gain	0
Observed Loss	144
Observed Complex	0
Frequency	n/a