fig3
![<i>EHMT1</i> pathogenic variants and 9q34.3 microdeletions share altered DNA methylation patterns in patients with Kleefstra syndrome](https://image.oaes.cc/0833dc0f-ab5f-4ae4-9da0-8669580bf27b/3507.fig.3.jpg)
Figure 3. Classification of additional samples with EHMT1 variants or deletions (n = 12) using KS signature. Output of SVM classification model trained on KS signature sites generating the probability of having KS for each sample. Samples classified include 12 individuals in unknown test or validation groups, 29 new controls, and 4 individuals with NCBRS. Horizontal line represents threshold for classifying samples as cases (above line) or controls (below line)