A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1919n54



Internal ID20135343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55603545..55631424hg38UCSC Ensembl
chr11:55371021..55398900hg19UCSC Ensembl
chr11:55127597..55155476hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3827880
hg1927880
hg1827880
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv554885, nsv554883
Samples
Known GenesOR4C11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1919n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss3
Observed Complex0
Frequencyn/a


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