Variant DetailsVariant: nsv9241 Internal ID | 15500467 | Landmark | | Location Information | | Cytoband | 15q14 | Allele length | Assembly | Allele length | hg38 | 203612 | hg19 | 203612 | hg18 | 203612 | hg17 | 203612 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv25279, nssv23543, nssv23562, nssv22294, nssv23598, nssv21916, nssv24363, nssv24337, nssv25304, nssv22515, nssv25329, nssv22277, nssv25602, nssv19999, nssv20572, nssv23478, nssv19720, nssv21302, nssv22863, nssv26120, nssv22466, nssv25322, nssv19775, nssv21946, nssv25926, nssv22495, nssv25254, nssv25905, nssv21546, nssv23570, nssv22892, nssv21976, nssv27452, nssv23590, nssv20201, nssv25625, nssv23506, nssv24510, nssv19690, nssv19660, nssv22525, nssv19805, nssv23534, nssv22130, nssv25297, nssv19835, nssv26101, nssv22158, nssv22406 | Samples | NA18502, NA11830, NA18980, NA07029, NA18504, NA12155, NA18563, NA12802, NA18860, NA18942, NA10839, NA19007, NA10847, NA10863, NA12872, NA18572, NA19221, NA18537, NA18853, NA19132, NA18517, NA18564, NA19240, NA19144, NA12740, NA18972, NA18552 | Known Genes | GOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2 | 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) | nsv9241
| Frequency | Sample Size | 31 | Observed Gain | 26 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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