Variant DetailsVariant: nssv451937Internal ID | 18275301 | Landmark | | Location Information | | Cytoband | 10q23.2 | Allele length | Assembly | Allele length | hg38 | 683147 | hg19 | 683147 | hg18 | 683147 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv428236 | Supporting Variants | | Samples | NA19257 | Known Genes | ADIRF, AGAP11, BMPR1A, FAM25A, FAM35A, GLUD1, LINC00864, LOC439994, MINPP1, MIR4678, MMRN2, NUTM2A, NUTM2A-AS1, NUTM2D, SNCG | 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) | nssv451937
| Frequency | Sample Size | 62 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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