Fig. 2From: Mapping the landscape of tandem repeat variability by targeted long read single molecule sequencing in familial X-linked intellectual disabilityChrX:45,606,270-45,606,355 tandem repeat (XLID25) is located downstream of MIR222. Sanger sequencing revealed the longest (CT)n sub-repeat in L020 XLID patient (5X17, bottom line), compared to 23 unaffected males. Co18 is the unaffected sibling (5X19) from the same L020 family.Back to article page