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Figure 5 | BMC Medical Genetics

Figure 5

From: Copy number variants (CNVs) analysis in a deeply phenotyped cohort of individuals with intellectual disability (ID)

Figure 5

Clustering of individuals based on 80 fine phenotypes. (A) Data displayed as heat map. K-means method was used to group the 78 individuals into two clusters. The filled dark squares indicate an abnormal phenotype. Statistically significant differences in the number of phenotype abnormalities were found between the two clusters (P < 0.05, Wilcoxon rank-sum test). The different groups of CNVs in each individual are indicated at the top of the heat map. ( B ) Data displayed as barplot. The prevalence of individuals with an abnormal phenotype was compared between the two clusters. *indicates P < 0.05 (Fisher exact test after multiple test corrections).

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