A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv920n71



Internal ID6318540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:350917..647869hg19UCSC Ensembl
chr11:340917..637869hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv896529, nsv896526, nsv896475, nsv896490, nsv896489, nsv896477, nsv896493, nsv896476, nsv896510, nsv896484, nsv896505, nsv896533, nsv896483
SamplesIS33684, IS33178, IS33248, IS37646, SP54956, IS37172, MS13095, IS35484, IS34304, MS19630, IS32737, IS40230, MS13727, IS38538, MS10698
Known GenesANO9, B4GALNT4, C11orf35, CDHR5, DEAF1, DRD4, HRAS, IRF7, LOC143666, LRRC56, MIR210, MIR210HG, PHRF1, PKP3, PTDSS2, RASSF7, RNH1, SCT, SIGIRR
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv920n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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