A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1911n54



Internal ID20135335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55600413..55641188hg38UCSC Ensembl
chr11:55367889..55408664hg19UCSC Ensembl
chr11:55124465..55165240hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3840776
hg1940776
hg1840776
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv554926, nsv554886, nsv554907, nsv554887, nsv554825, nsv554914, nsv554842, nsv554824
Samples
Known GenesOR4C11, OR4P4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1911n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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