A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv550570



Internal ID15559043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:65890789..66030069hg38UCSC Ensembl
Innerchr15:66183127..66322407hg19UCSC Ensembl
Innerchr15:63970181..64109461hg18UCSC Ensembl
Innerchr15:63898945..64038225hg16UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38139281
hg19139281
hg18139281
hg16139281
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv471684
Supporting Variants
SamplesNA10493
Known GenesMEGF11, RAB11A
MethodBAC aCGH
AnalysisArray image analysis and normalization were performed using UCSF Spot and Sproc software (Jain et al. 2002). BACs for which only one of the triplicates printed on the array yielded data, or for which the standard deviation of log2 ratio for the triplicates was 10.2, were removed from final analysis. Furthermore, we discarded BACs that failed to yield data in <20% of cases. For each hybridization experiment, we established a threshold log2 ratio of 2 SDs from the mean of all autosomal clones, and BACs that exceeded this threshold in both independent dye-swap experiments were classified as variant.
PlatformGPL4010
Comments
ReferenceSharp_et_al_2005
Pubmed ID15918152
Accession Number(s)nssv550570
Frequency
Sample Size48
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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