A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv935n71



Internal ID6318555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:541930..662407hg19UCSC Ensembl
chr11:531930..652407hg18UCSC 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 Variantsnsv896561, nsv896549, nsv896550
SamplesMS10386, IS35007, IS39233, MS18276, IS38403
Known GenesC11orf35, CDHR5, DEAF1, DRD4, IRF7, LOC143666, LRRC56, MIR210, MIR210HG, PHRF1, RASSF7, SCT
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv935n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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