Internal ID | 15201272 |
Landmark | |
Location Information | |
Cytoband | 20q11.22 |
Allele length | Assembly | Allele length | hg38 | 52701 | hg19 | 52701 | hg18 | 52701 | hg17 | 52701 |
|
Variant Type | CNV deletion |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | M |
Merged Variants | |
Supporting Variants | nssv2331, nssv4660, nssv1597 |
Samples | NA18555, NA19240, NA19129 |
Known Genes | |
Method | Sequencing |
Analysis | End-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005) |
Platform | Capillary |
Comments | |
Reference | Kidd_et_al_2008 |
Pubmed ID | 18451855 |
Accession Number(s) | nsv3357
|
Frequency | Sample Size | 9 | Observed Gain | 0 | Observed Loss | 3 | Observed Complex | 0 | Frequency | n/a |
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