Internal ID | 18274394 |
Landmark | |
Location Information | |
Cytoband | 10q23.2 |
Allele length | Assembly | Allele length | hg38 | 325848 | hg19 | 325848 | hg18 | 325848 |
|
Variant Type | CNV loss |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | S |
Merged Variants | nsv428236 |
Supporting Variants | |
Samples | HGDP01094 |
Known Genes | ADIRF, AGAP11, FAM25A, FAM35A, GLUD1, NUTM2A, NUTM2A-AS1 |
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) | nssv451941
|
Frequency | Sample Size | 62 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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