A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv832298



Internal ID16109481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:134062867..134110778hg38UCSC Ensembl
Outerchr11:133932762..133980673hg19UCSC Ensembl
Outerchr11:133437972..133485883hg18UCSC Ensembl
Outerchr11:133437972..133485883hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3847912
hg1947912
hg1847912
hg1747912
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv18n68
Supporting Variantsnssv1449539
Samples
Known GenesJAM3
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)nsv832298
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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