A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8873



Internal ID15846785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:114596838..114646692hg38UCSC Ensembl
Outerchr11:114467560..114517414hg19UCSC Ensembl
Outerchr11:113972770..114022624hg18UCSC Ensembl
Outerchr11:113972770..114022624hg17UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3849855
hg1949855
hg1849855
hg1749855
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv19584, nssv20455, nssv19976, nssv23585, nssv20505, nssv18622, nssv20298
SamplesNA18980, NA18942, NA18975, NA19007, NA18537, NA18564, NA18972
Known Genes
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nsv8873
Frequency
Sample Size31
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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