A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554815



Internal ID15995538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55594332..55618626hg38UCSC Ensembl
Innerchr11:55361808..55386102hg19UCSC Ensembl
Innerchr11:55118384..55142678hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3824295
hg1924295
hg1824295
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv775194
Samples
Known GenesOR4C11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554815
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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