A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554116



Internal ID16341525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:41796810..41806798hg38UCSC Ensembl
Innerchr11:41818360..41828348hg19UCSC Ensembl
Innerchr11:41774936..41784924hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg389989
hg199989
hg189989
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1763n54
Supporting Variantsnssv771644, nssv771643
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554116
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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