Variant DetailsVariant: nsv7173 Internal ID | 15205470 | Landmark | | Location Information | | Cytoband | 1p36.13 | Allele length | Assembly | Allele length | hg38 | 378741 | hg19 | 378741 | hg18 | 378741 | hg17 | 378741 |
| Variant Type | OTHER inversion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv9355, nssv10882, nssv5304, nssv3851, nssv3861, nssv5331, nssv3885, nssv10485, nssv10890, nssv10523, nssv11237, nssv10507, nssv747, nssv5314, nssv657, nssv1903, nssv929, nssv1777, nssv9691, nssv9682, nssv9405, nssv1910, nssv6334, nssv9949, nssv1863, nssv1893 | Samples | NA18507, NA12156, NA12878, NA18956, NA15510, NA18555, NA18517, NA19240, NA19129 | Known Genes | CROCC, CROCCP2, ESPNP, LOC729574, MIR3675, MST1L, MST1P2, NBPF1 | 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) | nsv7173
| Frequency | Sample Size | 9 | Observed Gain | 0 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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