| Panel name | UPD Chr.15 |
|---|---|
| Panel method | Genotyping |
| Panel version ** | None |
| Panel quality *** | |
| Core-NL | No core-NL genes included |
| CNV analysis | No |
| Note | UPD analyse Chr. 15 d.m.v. genotypering bij afwijkende methylering. UPD: bloed van beide ouders is noodzakelijk |
| Location | Location AMC |
| Genes (0) | Quality | % coverage >30 | % coverage >20 | Core-NL | Note |
|---|
| Indication(s) |
|---|
| Angelman syndrome AS |
| Angelman syndrome AS |
| Prader-Willi syndrome PWS |
| Prader-Willi syndrome PWS |
| Prader-Willi syndrome PWS |
** For information on previous versions of this panel, please contact the Genome Diagnostics Laboratory
*** NGS panel genes can be analyzed with different quality. More info about test quality type A, C or A/C