A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv936n71



Internal ID6318556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:551405..888632hg19UCSC Ensembl
chr11:541405..878632hg18UCSC 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 Variantsnsv896563, nsv896551
SamplesIS39258, IS31656, IS34235
Known GenesC11orf35, CD151, CDHR5, CEND1, CHID1, DEAF1, DRD4, EFCAB4A, EPS8L2, IRF7, LOC143666, LRRC56, MIR210, MIR210HG, PDDC1, PHRF1, PIDD, PNPLA2, POLR2L, RASSF7, RPLP2, SCT, SLC25A22, SNORA52, TALDO1, TMEM80, TSPAN4
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv936n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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