A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv428256



Internal ID18624706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55549600..55854408hg38UCSC Ensembl
Innerchr11:55317076..55621884hg19UCSC Ensembl
Innerchr11:55073652..55378460hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38304809
hg19304809
hg18304809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv452084, nssv452083
SamplesNA18916, NA19225
Known GenesOR4C11, OR4C15, OR4C16, OR4C6, OR4P4, OR4S2, OR5D13, OR5D14, OR5D16, OR5D18, OR5L1, OR5L2
MethodBAC aCGH
AnalysisCopy number variable segments were automatically detected using the CNVfinder algorithm (Fiegler et al. 2006).
PlatformSanger H. sapiens Whole Genome Tile Path 28.7k v3
Comments
ReferencePerry_et_al_2008b
Pubmed ID18775914
Accession Number(s)nsv428256
Frequency
Sample Size62
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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