Variant DetailsVariant: esv18980 | Internal ID | 11036214 | | Landmark | | | Location Information | | | Cytoband | 14q24.3 | | Allele length | | Assembly | Allele length | | hg38 | 57580 | | hg19 | 57580 | | hg18 | 57580 |
| | Variant Type | CNV gain | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | esv29080 | | Supporting Variants | essv43867, essv50679, essv69378, essv57196, essv44161, essv84028, essv66590, essv45188, essv61544, essv35818, essv35025, essv74229, essv68643, essv58081, essv59627, essv38230, essv62229, essv52358, essv42475, essv36873, essv33202, essv75582, essv75278, essv81475, essv56238, essv77687, essv70558, essv65059, essv80671, essv55005, essv49470, essv72227, essv47751, essv40643, essv39582 | | Samples | NA18502, NA11995, NA18861, NA12414, NA11931, NA12004, NA19190, NA18916, NA12287, NA12156, NA12044, NA12828, NA11993, NA12489, NA12878, NA18907, NA19114, NA11894, NA12239, NA15510, NA19099, NA19257, NA19225, NA06985, NA18523, NA18858, NA18909, NA19108, NA19147, NA18517, NA19240, NA18505, NA19129, NA12006, NA12776 | | Known Genes | ACOT1, ACOT2, HEATR4 | | Method | Oligo aCGH | | Analysis | Segment log2 ratios from each sample. This was done running the GADA algorithm (Pique-Regi et al., 2008) using the options "-M 10 -T 10 -a 2.5". Filter non-CNV segments using intensity thresholds. Merge remaining CNV "calls" within each sample. Adjacent calls of the same direction (gain or loss) are merged if both: the distance between calls is less than 10kb, and the distance between calls is less than 10% of the size of the largest of the two calls. | | Platform | Sanger H. Sapiens 42mCGH Array 5781_53 726K v1 | | Comments | | | Reference | Conrad_et_al_2009 | | Pubmed ID | 19812545 | | Accession Number(s) | esv18980
| | Frequency | | Sample Size | 40 | | Observed Gain | 35 | | Observed Loss | 0 | | Observed Complex | 0 | | Frequency | n/a |
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