A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1676238



Internal ID15187060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67748715..67910810hg38UCSC Ensembl
Innerchr11:67516186..67678281hg19UCSC Ensembl
Innerchr11:67272762..67434857hg18UCSC Ensembl
Innerchr11:67291546..67453641hg16UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38162096
hg19162096
hg18162096
hg16162096
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv469719
Supporting Variants
Samples
Known GenesFAM86C2P
MethodBAC aCGH
AnalysisA locus was considered a CNV if the log ratio of fluorescence measurements for the individuals assayed exceeded twice the SD of the autosomal clones in both dye-swapped experiments.
PlatformGPL4010
Comments
ReferenceLocke_et_al_2006
Pubmed ID16826518
Accession Number(s)nssv1676238
Frequency
Sample Size265
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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