A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1569n54



Internal ID18993745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2394970..2404870hg38UCSC Ensembl
chr11:2416200..2426100hg19UCSC Ensembl
chr11:2372776..2382676hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg389901
hg199901
hg189901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv553092, nsv553090, nsv553091
Samples
Known GenesCD81, TRPM5, TSSC4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1569n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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