A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554112



Internal ID16341521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:41796716..41807063hg38UCSC Ensembl
Innerchr11:41818266..41828613hg19UCSC Ensembl
Innerchr11:41774842..41785189hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3810348
hg1910348
hg1810348
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1763n54
Supporting Variantsnssv771632
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554112
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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