Table 3 Number of patients (total 20) with either a specific CNV for each cell fraction or a shared CNV detected in both cell fractions at the same location. Note that the shared amplifications detected at chromosome 3 and 14 represents a deletion in the reference DNA
Amplifications | Deletions | |||||
|---|---|---|---|---|---|---|
CD133 (20) | EpCAM (20) | Shared (20) | CD133 (20) | EpCAM (20) | Shared (20) | |
Chr 1 | 4 | 2 | 3 | 11 | 14 | 17 |
Chr 2 | 2 | 1 | 1 | 10 | 6 | 11 |
Chr 3 | 2 | 2 | 17 | 9 | 9 | 8 |
Chr 4 | 1 | 3 | 1 | 4 | 8 | 5 |
Chr 5 | 0 | 0 | 0 | 9 | 6 | 7 |
Chr 6 | 2 | 0 | 0 | 10 | 9 | 7 |
Chr 7 | 2 | 0 | 0 | 10 | 15 | 14 |
Chr 8 | 1 | 2 | 8 | 6 | 8 | 11 |
Chr 9 | 3 | 1 | 0 | 10 | 8 | 5 |
Chr 10 | 0 | 1 | 0 | 8 | 10 | 13 |
Chr 11 | 2 | 1 | 5 | 11 | 9 | 10 |
Chr 12 | 2 | 1 | 3 | 14 | 11 | 14 |
Chr 13 | 4 | 2 | 1 | 7 | 5 | 4 |
Chr 14 | 0 | 0 | 20 | 5 | 10 | 16 |
Chr 15 | 1 | 1 | 0 | 8 | 9 | 15 |
Chr 16 | 0 | 2 | 1 | 10 | 11 | 11 |
Chr 17 | 5 | 10 | 8 | 7 | 11 | 7 |
Chr 18 | 0 | 0 | 0 | 4 | 5 | 12 |
Chr 19 | 7 | 5 | 2 | 6 | 12 | 11 |
Chr 20 | 2 | 2 | 1 | 7 | 7 | 3 |
Chr 21 | 1 | 2 | 0 | 4 | 5 | 10 |
Chr 22 | 1 | 1 | 0 | 6 | 7 | 6 |