A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554034



Internal ID16341443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:38227656..38300656hg38UCSC Ensembl
Innerchr11:38249206..38322206hg19UCSC Ensembl
Innerchr11:38205782..38278782hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3873001
hg1973001
hg1873001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1749n54
Supporting Variantsnssv771097, nssv771100, nssv771093, nssv771094, nssv771101, nssv771099, nssv771095, nssv771096, nssv771102, nssv771098
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554034
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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