A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv832072



Internal ID16455941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:15205297..15370644hg38UCSC Ensembl
Outerchr11:15226843..15392190hg19UCSC Ensembl
Outerchr11:15183419..15348766hg18UCSC Ensembl
Outerchr11:15183419..15348766hg17UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38165348
hg19165348
hg18165348
hg17165348
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1449024
Samples
Known GenesINSC
MethodBAC aCGH
AnalysisExperimental SDs (SDautosome) were calculated for each experiment on the basis of the log2 ratios of the 24,392 reliable clones minus the clones removed because of low signal-to-noise ratio (SNR) or high SD of replicate clone measures (SDclone). Thresholds for determining CNV clones were set at a multiple of the SDautosome value. For each experiment, clones were annotated as uninformative if they were filtered via SNR or SDclone, as a CNV loss if the log2 ratio was less than the negative threshold, as unchanged if the log2 ratio was between the negative and positive thresholds, and as a CNV gain if the log2 ratio was above the positive threshold.
PlatformGPL2616
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nsv832072
Frequency
Sample Size95
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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