A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv832106



Internal ID16455975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:31217866..31408189hg38UCSC Ensembl
Outerchr11:31239413..31429736hg19UCSC Ensembl
Outerchr11:31195989..31386312hg18UCSC Ensembl
Outerchr11:31195989..31386312hg17UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38190324
hg19190324
hg18190324
hg17190324
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1449086, nssv1449081, nssv1449083, nssv1449090, nssv1449080, nssv1449092, nssv1449082, nssv1449085, nssv1449091, nssv1449093, nssv1449087, nssv1449079, nssv1449088, nssv1449089
Samples
Known GenesDCDC1, DNAJC24
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)nsv832106
Frequency
Sample Size95
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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