One of the comments below the article:
Gary Smith says: Twins "start with identical genes, because each is formed from a single fertilised egg that splits into two embryos. But from that moment onwards, their DNA begins diverging. The DNA replication mechanism introduces about one new mutation for every 100 million base pairs copied, per generation.
There are around three billion base pairs in the human genome, so you would expect between 10 and 100 new mutations per person that occur early enough in embryonic development to be present in most cells in the body. Ordinary DNA tests won’t normally detect this because they only examine a short section of the DNA, in a region known to be highly variable between individuals. But if the entire genome were sequenced, these differences would show up."
I have no idea if that is a reasonable hypothesis or not........