Variant DetailsVariant: nsv6895Internal ID | 15205164 | Landmark | | Location Information | | Cytoband | Xp11.23 | Allele length | Assembly | Allele length | hg38 | 4374 | hg19 | 4374 | hg18 | 4374 | hg17 | 4374 |
| Variant Type | CNV insertion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv3785 | Samples | NA12878 | Known Genes | CACNA1F, CCDC22, FOXP3 | 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) | nsv6895
| Frequency | Sample Size | 9 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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