A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666582



Internal ID9586001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55598240..55690746hg38UCSC Ensembl
Outerchr11:55597869..55691116hg38UCSC Ensembl
Innerchr11:55365716..55458222hg19UCSC Ensembl
Outerchr11:55365345..55458592hg19UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3893248
hg1993248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv211e199
Supporting Variantsessv6083506, essv5959121, essv6108677, essv5413096, essv6354122, essv6085900, essv6545710, essv5628742, essv6553406, essv5467691, essv6491017, essv5497931, essv6240138, essv6577937, essv6119074, essv6393648, essv6164642, essv6198858, essv6287734, essv6004049, essv6025347, essv6055745, essv5454127, essv6380959, essv5883996, essv5403848, essv5804935, essv6277032, essv6088782, essv5525827, essv6235761, essv5583946, essv5661947, essv5545657, essv6175668, essv6389405, essv6396781, essv6117674, essv5667681, essv5533890, essv5493832, essv5942435, essv5951140, essv5636696, essv6241878, essv5789431, essv6459324, essv6459288, essv6104740, essv5851520, essv5699328, essv5962102, essv5591847
SamplesNA20761, NA20766, NA20508, NA20783, NA20816, NA20532, NA20512, NA20805, NA20507, NA20814, NA20537, NA20796, NA20798, NA20589, NA20774, NA20795, NA20769, NA20768, NA20540, NA20539, NA20518, NA20819, NA20812, NA20811, NA20533, NA20515, NA20535, NA20524, NA20505, NA20521, NA20810, NA20760, NA20525, NA20581, NA20538, NA20522, NA20801, NA20815, NA20804, NA20520, NA20530, NA20527, NA20778, NA20504, NA20544, NA20797, NA20582, NA20786, NA20758, NA20503, NA20502, NA20754, NA20509
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666582
Frequency
Sample Size1151
Observed Gain0
Observed Loss53
Observed Complex0
Frequencyn/a


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