Trisomy 21 is the type of Down Syndrome that is usually caused by in meiosis called disjunction. Nondisjunction results in the extra copy of chromosome 21 when a pair of chromosome 21 in the sperm or egg fails to separate. As the unborn offspring develops, the extra chromosome is copied to every cell of its body. This type of Down Syndrome, trisomy 21, occurs 95% of Down Syndromes inheritances. Another type of Down Syndrome is mosaicism. Mosaicism takes place when there is a combination of two types of cells. One cell has the normal 46 chromosomes and the other have 47 chromosomes (contains the extra chromosome 21). This type of Down Syndrome is the least common type-it is about 1% of all Down Syndrome cases. Research indicates that people with this type of Down Syndrome have less characteristics of the disorder than other types. The last and final type of Down Syndrome is called translocation. In translocation, the chromosomes are the normal 46, but an additional chromosome 21 attaches to another chromosome, usually number 14. The appearance or presence of the chromosome gives the organism the characteristics of Down