A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1946n54



Internal ID22769841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55927680..55941339hg38UCSC Ensembl
chr11:55695156..55708815hg19UCSC Ensembl
chr11:55451732..55465391hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3813660
hg1913660
hg1813660
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv555086, nsv555085
Samples
Known GenesOR5I1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1946n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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