Variant DetailsVariant: nsv3861Internal ID | 15201827 | Landmark | | Location Information | | Cytoband | 3p14.1 | Allele length | Assembly | Allele length | hg38 | 5891 | hg19 | 5891 | hg18 | 5891 | hg17 | 5891 |
| Variant Type | CNV insertion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv306, nssv7821 | Samples | NA12156, NA19240 | Known Genes | FAM19A1 | Method | Sequencing | Analysis | End-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005) | Platform | Capillary | Comments | | Reference | Kidd_et_al_2008 | Pubmed ID | 18451855 | Accession Number(s) | nsv3861
| Frequency | Sample Size | 9 | Observed Gain | 2 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|
|