Internal ID | 15205969 |
Landmark | |
Location Information | |
Cytoband | 10q26.3 |
Allele length | Assembly | Allele length | hg38 | 10124 | hg19 | 10124 | hg18 | 10124 | hg17 | 10124 |
|
Variant Type | CNV insertion |
Copy Number | |
Allele State | |
Allele Origin | |
Probe Count | |
Validation Flag | |
Merged Status | M |
Merged Variants | |
Supporting Variants | nssv9936, nssv6427, nssv3910 |
Samples | NA18507, NA12156, NA12878 |
Known Genes | LRRC27 |
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) | nsv7627
|
Frequency | Sample Size | 9 | Observed Gain | 3 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
|