A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554211



Internal ID15994934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:48084934..48673319hg38UCSC Ensembl
Innerchr11:48106486..48694871hg19UCSC Ensembl
Innerchr11:48063062..48651447hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38588386
hg19588386
hg18588386
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174784
Samples1780862521_A
Known GenesOR4A47, OR4B1, OR4C3, OR4C45, OR4S1, OR4X1, OR4X2, PTPRJ
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554211
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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