A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555171



Internal ID15995894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:61848540..61897520hg38UCSC Ensembl
Innerchr11:61616012..61664992hg19UCSC Ensembl
Innerchr11:61372588..61421568hg18UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3848981
hg1948981
hg1848981
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174804
Samples1780854206_A
Known GenesFADS2, FADS3, MIR6746, RAB3IL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555171
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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