Variant DetailsVariant: nsv7435Internal ID | 15205758 | Landmark | | Location Information | | Cytoband | 9q33.2 | Allele length | Assembly | Allele length | hg38 | 93044 | hg19 | 93044 | hg18 | 93044 | hg17 | 93044 |
| Variant Type | OTHER inversion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv9474, nssv11205, nssv3750, nssv10682, nssv11204, nssv10683, nssv3749, nssv6296, nssv6297 | Samples | NA12156, NA12878, NA18956, NA15510, NA18517 | Known Genes | LHX2 | 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) | nsv7435
| Frequency | Sample Size | 9 | Observed Gain | 0 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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