A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1675902



Internal ID15533410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4165751..4315260hg38UCSC Ensembl
Innerchr11:4186981..4336490hg19UCSC Ensembl
Innerchr11:4143557..4293066hg18UCSC Ensembl
Innerchr11:4151290..4300799hg16UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38149510
hg19149510
hg18149510
hg16149510
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv469627
Supporting Variants
Samples
Known GenesLOC100506082
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)nssv1675902
Frequency
Sample Size265
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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