clinical symptoms

In general 70% of sSMC carriers are clinically normal. The figures listed above
are based on the bias, that mainly clinically aberrant cases are studied and reported in literature!

UPD (uniparental disomy) cases:

UPD(10)mat

UPD(10)pat

UPD(10)mat or pat

the probably non-dosage sensitive pericentric region of chromosome 10
schematic cytogenetic depiction	short (= p-) arm het long (= q-) arm p14 p13 p12 p11.2 cen q11.2 q21 q22 no clinical signs clinical signs
schematic molecular- cytogenetic depiction	Data is converted between genome versions by UCSC browser! Note the changes defined there for centromere-sizes; due to that and due to 'new insertions and deletions', positions are not always seeming logical comparing different versions listed  genomic version critical region p-arm uncritical region p-arm centromere uncritical region q-arm critical region q-arm NCBI 36/ hg18 34.46 34.75 38.80 - 42.10 51.79 unknown GRCh 37/ hg19 34.42 34.71 38.00 - 42.30 52.12 unknown GRCh 38/ hg38 34.13 34.42 38.00 - 41.60 50.36 unknown   Positions given in megabasepair (Mbp) acc. to cases marked as ***