Variant DetailsVariant: nsv10617 Internal ID | 15498894 | Landmark | | Location Information | | Cytoband | 1p13.3 | Allele length | Assembly | Allele length | hg38 | 40432 | hg19 | 40432 | hg18 | 40432 | hg17 | 40432 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv16742, nssv18432, nssv17094, nssv23079, nssv16426, nssv16429, nssv16102, nssv19769, nssv20099, nssv17410, nssv23389, nssv17402, nssv17080, nssv17740, nssv14755, nssv20744, nssv16432, nssv17072, nssv15753, nssv16083, nssv15095, nssv20100, nssv17415, nssv17745, nssv18771, nssv21074, nssv23699, nssv16438, nssv17747, nssv15777, nssv17101, nssv17090 | Samples | NA18502, NA18980, NA07029, NA18563, NA12802, NA18860, NA18942, NA07048, NA18975, NA10847, NA18572, NA19221, NA18537, NA18853, NA19132, NA18517, NA19240, NA19144, NA19173, NA18972, NA18552 | Known Genes | GSTM1, GSTM2, GSTM5 | Method | Oligo aCGH | Analysis | Statistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2 | Platform | Agilent-015686 Custom Human 244K CGH Microarray | Comments | | Reference | Perry_et_al_2008 | Pubmed ID | 18304495 | Accession Number(s) | nsv10617
| Frequency | Sample Size | 31 | Observed Gain | 21 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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