A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv832299



Internal ID16109482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:134170258..134346785hg38UCSC Ensembl
Outerchr11:134040153..134216679hg19UCSC Ensembl
Outerchr11:133545363..133721889hg18UCSC Ensembl
Outerchr11:133545363..133721889hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38176528
hg19176527
hg18176527
hg17176527
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1449542, nssv1449543, nssv1449541
Samples
Known GenesACAD8, GLB1L2, GLB1L3, NCAPD3, THYN1, VPS26B
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)nsv832299
Frequency
Sample Size95
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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