A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1910n54



Internal ID20135334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55600413..55634231hg38UCSC Ensembl
chr11:55367889..55401707hg19UCSC Ensembl
chr11:55124465..55158283hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3833819
hg1933819
hg1833819
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv554818, nsv554865, nsv554822, nsv554821, nsv554823, nsv554841, nsv554820, nsv554925
Samples
Known GenesOR4C11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1910n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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