Variant DetailsVariant: nsv828723 | Internal ID | 16091197 | | Landmark | | | Location Information | | | Cytoband | 20q12 | | Allele length | | Assembly | Allele length | | hg38 | 1185 | | hg19 | 1185 | | hg18 | 1185 |
| | Variant Type | CNV loss | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | dgv700n67 | | Supporting Variants | nssv1422304, nssv1425440, nssv1427961, nssv1435578, nssv1439397, nssv1434813, nssv1433364, nssv1427179, nssv1437149, nssv1437029, nssv1428760, nssv1434111, nssv1429516, nssv1438536, nssv1440065, nssv1431442, nssv1424683, nssv1431751, nssv1423435, nssv1432579, nssv1426300, nssv1422452, nssv1423887, nssv1430962, nssv1440765, nssv1430268, nssv1431030, nssv1437871, nssv1423056 | | Samples | AK2, NA18947, AK16, NA18592, AK20, NA18999, NA18526, NA18969, AK10, AK6, NA18547, NA18942, NA18582, NA18949, AK14, AK8, NA18973, NA18951, NA18537, NA18570, NA18542, NA18564, AK18, AK12, AK4, NA18972, NA18552, NA18968, NA18997 | | Known Genes | ZHX3 | | Method | Oligo aCGH | | Analysis | To select parameters for calling CNVs (that is, the statistical threshold of the ADM2 algorithm, the minimum +/- log2 ratio and the minimum number of consecutive probes in a CNV interval), we calculated the sensitivity and positive predictive value based on the comparison of aCGH-based CNV calls (using our high-resolution Agilent 24M platform) with read-depth sequence data for two samples from Korean individuals (AK1 and AK2). We attempted to obtain `absolute' copy number status of the sample from NA10851, which was used as the reference sample for aCGH experiments in this study. For this, we used read-depth data for NA10851 obtained from massively parallel sequencing by the Illumina GA II data. The read-depth data represent the copy number status of NA10851 as compared to the human reference genome (hg18) because the short read sequences were aligned to hg18. | | Platform | Agilent 24M aCGH | | Comments | | | Reference | Park_et_al_2010 | | Pubmed ID | 20364138 | | Accession Number(s) | nsv828723
| | Frequency | | Sample Size | 31 | | Observed Gain | 0 | | Observed Loss | 29 | | Observed Complex | 0 | | Frequency | n/a |
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