Internal ID | 18275314 |
Landmark | |
Location Information | |
Cytoband | 22q11.21 |
Allele length | Assembly | Allele length | hg38 | 711555 | hg19 | 216302 | hg18 | 216302 |
|
Variant Type | CNV loss |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | S |
Merged Variants | nsv428385 |
Supporting Variants | |
Samples | NA19257 |
Known Genes | GGT3P, PEX26, TUBA8, USP18 |
Method | BAC aCGH |
Analysis | Copy number variable segments were automatically detected using the CNVfinder algorithm (Fiegler et al. 2006). |
Platform | Sanger H. sapiens Whole Genome Tile Path 28.7k v3 |
Comments | |
Reference | Perry_et_al_2008b |
Pubmed ID | 18775914 |
Accession Number(s) | nssv453961
|
Frequency | Sample Size | 62 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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