Variant DetailsVariant: nsv9397 Internal ID | 15500623 | Landmark | | Location Information | | Cytoband | 16p12.1 | Allele length | Assembly | Allele length | hg38 | 323623 | hg19 | 323623 | hg18 | 323623 | hg17 | 323623 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv22608, nssv22859, nssv22783, nssv25934, nssv26687, nssv24032, nssv22578, nssv27790, nssv20255, nssv25913, nssv20801, nssv22383, nssv21842, nssv23647, nssv26078, nssv25221, nssv22637, nssv22995, nssv24122, nssv20200, nssv26266 | Samples | NA18980, NA07029, NA18504, NA12155, NA18563, NA12802, NA18860, NA07048, NA10839, NA10847, NA12872, NA19221, NA19132, NA18517, NA18564, NA19144, NA19173, NA18972, NA18552 | Known Genes | IGSF6, LOC100271836, METTL9, OTOA, RRN3P1, SLC7A5P2 | 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) | nsv9397
| Frequency | Sample Size | 31 | Observed Gain | 18 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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