A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8807



Internal ID15500033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:34890620..34908742hg38UCSC Ensembl
Outerchr11:34912167..34930289hg19UCSC Ensembl
Outerchr11:34868743..34886865hg18UCSC Ensembl
Outerchr11:34868743..34886865hg17UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3818123
hg1918123
hg1818123
hg1718123
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv22993
SamplesNA18972
Known GenesAPIP
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)nsv8807
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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