Variant DetailsVariant: nsv9238 Internal ID | 15500464 | Landmark | | Location Information | | Cytoband | 15q13.3 | Allele length | Assembly | Allele length | hg38 | 456201 | hg19 | 456201 | hg18 | 456201 | hg17 | 456201 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv27369, nssv24484, nssv25556, nssv21886, nssv25579, nssv27444, nssv23458, nssv25272, nssv23515, nssv25229, nssv23430, nssv22376, nssv27378, nssv19969, nssv25863, nssv27435, nssv22346, nssv23487, nssv25884, nssv22316, nssv23514, nssv23459, nssv23486, nssv27426, nssv27387, nssv23431 | Samples | NA18502, NA11830, NA12155, NA19007, NA18572, NA19221, NA19132, NA18517, NA19240, NA18972, NA18552 | Known Genes | CHRNA7, GOLGA8K, GOLGA8O, GOLGA8R, LOC100996255, ULK4P1, ULK4P2, ULK4P3, WHAMMP1 | 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) | nsv9238
| Frequency | Sample Size | 31 | Observed Gain | 4 | Observed Loss | 8 | Observed Complex | 0 | Frequency | n/a |
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