Table 2.
Profile of five pathogenic microdeletions.
| Case | Chromosomal position (hg19) | Size (Mb) | Involved epilepsy genes | Onset | Electroclinical syndrome |
|---|---|---|---|---|---|
| Case 92 | Chr2:165755330-168986256 | 3.23 | SCN2A, SCN1A, SCN9A | 2 months | Dravet syndrome |
| Case 16 | Chr16:29652999-30198600 | 0.54 | PRRT2 | 4 months | Unclassified |
| Case 32 | Chr16:29673954-30119759 | 0.44 | PRRT2 | 4 days | Benign infantile epilepsy |
| Case 18 | Chr20:61472348-62281707 | 0.80 | CHRNA4, KCNQ2 | 2 months | Unclassified |
| Case 80 | Chr20:61845191-62065069 | 0.21 | CHRNA4, KCNQ2 | 1 day | Benign infantile epilepsy |